Material for organic electronic device, and organic electronic device using same

ABSTRACT

The present invention provides a novel compound that is capable of largely improving a life time, efficiency, electrochemical stability, and thermal stability of an organic electronic device, and an organic electronic device that comprises an organic material layer comprising the compound.

This application is a continuation of and claims the benefit of U.S.application Ser. No. 13/060,248, filed May 18, 2011, which is a NationalStage Application of PCT/KR2009/004689, filed Aug. 21, 2009, whichclaims the benefit of Korean Patent Application No. 10-2008-0082477,filed Aug. 22, 2008, all of which are incorporated by reference in theirentirety herein.

TECHNICAL FIELD

The present invention relates to a novel compound that is capable oflargely improving a life time, efficiency, electrochemical stability,and thermal stability of an organic electronic device, and an organicelectronic device using the same.

BACKGROUND ART

An organic light emission phenomenon is an example of a conversion ofcurrent into visible rays through an internal process of a specificorganic molecule. The organic light emission phenomenon is based on thefollowing mechanism. When organic material layers are interposed betweenan anode and a cathode, if voltage is applied between the twoelectrodes, electrons and holes are injected from the cathode and theanode into the organic material layer. The electrons and the holes whichare injected into the organic material layer are recombined to form anexciton, and the exciton is reduced to a bottom state to emit light. Anorganic light emitting device which is based on the above mechanismtypically comprises a cathode, an anode, and organic material layer(s)interposed between thereof, for example, organic material layerscomprising a hole injection layer, a hole transport layer, a lightemitting layer, and an electron transport layer, interposedtherebetween.

The materials used in the organic light emitting device are mostly pureorganic materials or complexes of organic material and metal. Thematerial used in the organic light emitting device may be classified asa hole injection material, a hole transport material, a light emittingmaterial, an electron transport material, or an electron injectionmaterial, according to its use. In connection with this, an organicmaterial having a p-type property, which is easily oxidized and iselectrochemically stable when it is oxidized, is mostly used as the holeinjection material or the hole transport material. Meanwhile, an organicmaterial having an n-type property, which is easily reduced and iselectrochemically stable when it is reduced, is used as the electroninjection material or the electron transport material. As the lightemitting layer material, a material having both p-type and n-typeproperties is preferable, which is stable when it is oxidized and whenit is reduced. Also a material having high light emission efficiency forconversion of the exciton into light when the exciton is formed ispreferable.

In addition, it is preferable that the material used in the organiclight emitting device further have the following properties.

First, it is preferable that the material used in the organic lightemitting device have excellent thermal stability. The reason is thatjoule heat is generated by movement of electric charges in the organiclight emitting device. NPB, which has recently been used as the holetransport layer material, has a glass transition temperature of 100° C.or lower, thus it is difficult to apply to an organic light emittingdevice requiring a high current.

Second, in order to produce an organic light emitting device that iscapable of being actuated at low voltage and has high efficiency, holesand electrons which are injected into the organic light emitting devicemust be smoothly transported to a light emitting layer, and must not bereleased out of the light emitting layer. To achieve this, a materialused in the organic light emitting device must have a proper band gapand a proper HOMO or LUMO energy levels. A LUMO energy level ofPEDOT:PSS, which is currently used as a hole transport material of anorganic light emitting device produced using a solution coating method,is lower than that of an organic material used as a light emitting layermaterial, thus it is difficult to produce an organic light emittingdevice having high efficiency and a long lifespan.

Moreover, the material used in the organic light emitting device musthave excellent chemical stability, electric charge mobility, andinterfacial characteristic with an electrode or an adjacent layer. Thatis to say, the material used in the organic light emitting device mustbe little deformed by moisture or oxygen. Furthermore, proper hole orelectron mobility must be assured so as to balance densities of theholes and of the electrons in the light emitting layer of the organiclight emitting device to maximize the formation of excitons.Additionally, it has to be able to have a good interface with anelectrode comprising metal or metal oxides so as to assure stability ofthe device.

Accordingly, there is a need to develop an organic material having theabove-mentioned requirements in the art.

DISCLOSURE Technical Problem

Therefore, the present inventors aim to provide a novel compound that iscapable of satisfying conditions required of a material which may beused for an organic light emitting device and an organic electronicdevice, for example, a proper energy level, electrochemical stability,and thermal stability, and is capable of largely improving a life timeand efficiency of the organic electronic device, and an organicelectronic device using the same.

Technical Solution

The present invention provides a compound that is represented by thefollowing Formula 1:

wherein R¹ and R² are bonded to each other to form an aromatic ring orR³ and R⁴ are bonded to each other to form an aromatic ring, or R¹ andR² are bonded to each other to form an aromatic ring while R³ and R⁴ arebonded to each other to form an aromatic ring,

at least one of a group at which an aromatic ring is not formed among R⁵to R⁸, R¹ to R⁴, a substituent group that is substituted at an aromaticring that is formed by bonding R¹ and R² to each other, and asubstituent group that is substituted at an aromatic ring that is formedby bonding R³ and R⁴ to each other is -(L1)p-(Y1)q, p is an integer inthe range of 0 to 10, and q is an integer in the range of 1 to 10,

the remains are each independently -(L2)r-(Y2)s, r is an integer in therange of 0 to 10, and s is an integer in the range of 1 to 10,

X is -(A)_(m)-(B)_(n), m is an integer in the range of 0 to 10, and n isindependently an integer in the range of 1 to 10,

A is a substituted or unsubstituted arylene group; a substituted orunsubstituted alkenylene group; a substituted or unsubstitutedfluorenylene group; or a substituted or unsubstituted heteroarylenegroup that comprises one or more of N, O and S atoms,

in the case of when m is 0, B is hydrogen; deuterium; substituted orunsubstituted alkyl group; substituted or unsubstituted alkenyl group;substituted or unsubstituted silyl group; substituted or unsubstitutedboron group; substituted or unsubstituted aryl group having 6 to 30carbon atoms; substituted or unsubstituted fluorenyl group; orsubstituted or unsubstituted hetero ring group having one or more of N,O, and S atoms; in the case of when m is not 0, B is hydrogen;deuterium; halogen group; nitrile group; nitro group; hydroxy group;substituted or unsubstituted alkyl group; substituted or unsubstitutedcycloalkyl group; substituted or unsubstituted alkoxy group; substitutedor unsubstituted aryloxy group; substituted or unsubstituted alkylthioxygroup; substituted or unsubstituted arylthioxy group; substituted orunsubstituted alkylsulfoxy group; substituted or unsubstitutedarylsulfoxy group; substituted or unsubstituted alkenyl group;substituted or unsubstituted silyl group; substituted or unsubstitutedboron group; substituted or unsubstituted aryl group having 6 to 30carbon atoms; substituted or unsubstituted fluorenyl group; orsubstituted or unsubstituted hetero ring group having one or more of N,O, and S atoms,

L1 and L2 are the same as or different from each other, and are eachindependently substituted or unsubstituted arylene group; substituted orunsubstituted alkenylene group; substituted or unsubstitutedfluorenylene group; substituted or unsubstituted carbazolylene group; orsubstituted or unsubstituted heteroarylene group having one or more ofN, O, and S atoms,

Y1 is —N(Z1)(Z2), substituted or unsubstituted carbazole group, orsubstituted or unsubstituted benzocarbazole group,

Z1 and Z2 are the same as or different from each other, and are eachindependently substituted or unsubstituted alkyl group; substituted orunsubstituted cycloalkyl group, substituted or unsubstituted aryl group;substituted or unsubstituted alkenyl group; substituted or unsubstitutedfluorenyl group; substituted or unsubstituted carbazolyl group; orsubstituted or unsubstituted hetero ring group having one or more of N,O, and S atoms,

Y2 is hydrogen; deuterium; halogen group; nitrile group; nitro group;hydroxy group; substituted or unsubstituted alkyl group; substituted orunsubstituted cycloalkyl group; substituted or unsubstituted alkoxygroup; substituted or unsubstituted aryloxy group; substituted orunsubstituted alkylthioxy group; substituted or unsubstituted arylthioxygroup; substituted or unsubstituted alkylsulfoxy group; substituted orunsubstituted arylsulfoxy group; substituted or unsubstituted alkenylgroup; substituted or unsubstituted silyl group; substituted orunsubstituted boron group; substituted or unsubstituted alkylaminegroup; substituted or unsubstituted aralkylamine group; substituted orunsubstituted arylamine group; substituted or unsubstituted aryl group;substituted or unsubstituted fluorenyl group; substituted orunsubstituted carbazole group; or substituted or unsubstitutedcarbazolyl group; or substituted or unsubstituted hetero ring grouphaving one or more of N, O, and S atoms; and

in the case of when two or more A, B, L1, L2, Y1 or Y2 are provided,they may be the same as or different from each other, and thesubstituent groups may form an aliphatic or hetero condensation ring inconjunction with an adjacent group.

In the present invention, Formula 1 may be represented by the followingFormulas 2 to 4.

In the case of when R¹ and R² are bonded to each other to form anaromatic ring, it may be represented by the following Formula 2.

In the case of when R³ and R⁴ are bonded to each other to form anaromatic ring, it may be represented by the following Formula 3.

In the case of when R¹ and R² are bonded to each other to form anaromatic ring and R³ and R⁴ are bonded to each other to form an aromaticring, it may be represented by the following Formula 4.

In Formulas 2 to 4, X and R⁵ to R⁸ are the same as those defined byFormula 1, at least one of R′ and R″ is -(L1)p-(Y1)q, the remains areeach independently -(L2)r-(Y2)s, and X, L1, L2, Y1, Y2, p, q, r and sare the same as those defined by Formula 1.

In addition, the present invention provides an organic electronic devicecomprising a first electrode; a second electrode; and one or moreorganic material layers that are disposed between the first electrodeand the second electrode, wherein one or more layers of the organicmaterial layers comprises the compound that is represented by Formula 1.

Advantageous Effects

A compound according to the present invention may be used as an organicmaterial layer material, for example, a hole injection material, a holetransport material, a light emitting material, an electron transportmaterial, an electron injection material and the like, and particularly,a hole injection material and/or a hole transport material in an organicelectronic device. In the case of when the compound according to thepresent invention is used in the organic light emitting device and theorganic electronic device, a driving voltage of the device may bereduced, light efficiency may be improved, and a life time property ofthe device may be improved because of thermal stability of the compound.

DESCRIPTION OF DRAWINGS

FIG. 1 illustrates an example of an organic light emitting device thatcomprises a substrate 1, an anode 2, a light emitting layer 3, and acathode 4.

FIG. 2 illustrates an example of an organic light emitting device thatcomprises a substrate 1, an anode 2, a hole injection layer 5, a holetransport layer 6, a light emitting layer 7, an electron transport layer8, and a cathode 4.

FIG. 3 is a mass spectrum of a compound that is represented by Formula1-1-1.

FIG. 4 is a mass spectrum of a compound that is represented by Formula3-1-1.

FIG. 5 is a mass spectrum of a compound that is represented by Formula1-21-1.

FIG. 6 is a mass spectrum of a compound that is represented by Formula3-21-1.

FIG. 7 is a mass spectrum of a compound that is represented by Formula1-101-1.

FIG. 8 is a mass spectrum of a compound that is represented by Formula3-101-1.

FIG. 9 is 1H-NMR spectrum of the intermediate compound 4B-2.

FIG. 10 is 1H-NMR spectrum of the intermediate compound 2C-2.

BEST MODE

Hereinafter, the present invention will be described in detail.

The compound according to the present invention is characterized in thatit is represented by Formula 1.

In Formula 1, an alkyl group, an alkoxy group, and an alkenyl group maybe a straight chain or a branched chain. The number of carbon atoms ofthe alkyl group, the alkoxy group, and the alkenyl group is notparticularly limited, but it is preferable that it is in the range of 1to 30, which is the range that does not provide sterical hindrance. Forexample, in the case of when L1 or L2 of Formula 1 is the alkyl group,since it affects the application method to the organic electron deviceof the compound, for example, the application of the vacuum depositionmethod or the solution coating method, the number of carbon atoms of thealkyl group is not particularly limited.

In Formula 1, the cycloalkyl group is not particularly limited, but ithas preferably the number of carbon atoms in the range of 3 to 60, andit is particularly preferable that it is the cyclopentyl group and thecyclohexyl group.

In the present invention, as the alkenyl group, the alkenyl group having2 to 40 carbon atoms is preferable, and in detail, the alkenyl groupthat is substituted with the aryl group, such as the stylbenzyl group,the styrenyl group and the like is preferable, but it is not limitedthereto.

In Formula 1, the aryl group may be a monocycle or a polycycle, and thenumber of carbon atoms is not particularly limited, but it is preferablethat it is in the range of 6 to 30. As examples of the monocyclic arylgroup, there are the phenyl group, the biphenyl group, the terphenylgroup, stilbene and the like, and as examples of the polycyclic arylgroup, there are the naphthyl group, the anthryl group, the phenanthrylgroup, the pyrenyl group, the perylenyl group, the crycenyl group andthe like, but the scope of the present invention is not limited thereto.

In Formula 1, the hetero ring group is a ring group having a heteroatomof O, N or S, and the number of carbon atoms is not particularlylimited, but it is preferable that the number of carbon atoms is in therange of 3 to 60. As examples of the hetero ring group, there are athiophene group, a furane group, a pyrol group, an imidazole group, athiazol group, an oxazol group, an oxadiazol group, a triazol group, apyridyl group, a pyridazine group, a quinolynyl group, an isoquinolinegroup, an acrydyl group and the like, and the compounds that have thefollowing Structural Formulas are preferable, but they are not limitedthereto.

In Formula 1, the cycloalkyl group is not particularly limited, but ithas preferably the number of carbon atoms in the range of 3 to 60. Asexamples of the cycloalkyl group, there are the cyclopentyl group, thecyclohexyl group and the like, but it is not limited thereto.

In the present invention, as examples of the halogen group, there arefluorine, chlorine, bromine, or iodine.

In Formula 1, it is preferable that the fluorenyl group is the compoundof the following Structural Formulas, but it is not limited thereto.

In Formula 1, “substituted or unsubstituted” means that it issubstituted by one or more substituent groups that are selected from thegroup consisting of deuterium, halogen group, nitrile group, nitrogroup, hydroxy group, alkyl group, cycloalkyl group, alkenyl group,alkoxy group, aryloxy group, thioxy group, alkylthioxy group, arylthioxygroup, sulfoxy group, alkylsulfoxy group, arylsulfoxy group, silylgroup, boron group, arylamine group, aralkylamine group, alkylaminegroup, aryl group, fluorenyl group, carbazole group, arylalkyl group,arylalkenyl group, hetero ring group and acetylene group, or it does nothave any substituent group.

In Formula 1, with respect to X, in the case of when m is not 0, it ispreferable that A is the arylene group, the fluorenylene group or theheteroarylene group, and B is hydrogen, deuterium, fluorine, the alkylgroup, the cycloalkyl group, the silyl group, the aryl group, thefluorenyl group or the hetero ring group.

In Formula 1, it is preferable that R5 is hydrogen.

In Formulas 2 to 4, it is preferable that at least one of R6 to R8 or R′to R″ is -(L1)p-(Y1)q, p and q are not 0, L1 is the arylene group, thefluorenylene group, the carbazolylene group or the heteroarylene group,and Y1 is —N(Z1)(Z2), the substituted or unsubstituted carbazole group,or the substituted or unsubstituted benzocarbazole group.

In Formula 1 to Formula 4, in the case of when A of X is the arylenegroup, it is preferable that it is the phenylene group, the biphenylenegroup, the naphthalenyl group, the binaphthalene group, theanthracenylene group, the fluorenylene group, the crycenylene group, andthe phenanthrenylene group.

In Formula 1 to Formula 4, in the case of when A of X is the arylenegroup, it is preferable that it is C6˜C30 arylene group.

In Formula 1 to Formula 4, in the case of when A of X is theheteroarylene group, it is preferable that it is the imidazolylenegroup, the oxazolylene group, the thiazolylene group, the triazylenegroup, the pyridylene group, the pyrimidylene group, the quinolylenegroup, the carbazolylene group, and the indolyzylene group.

In Formula 1 to Formula 4, in the case of when B of X is the alkyl groupand the cycloalkyl group, it is preferable that B is the methyl group,the propyl group, butyl, and the cyclohexyl group.

In Formula 1 to Formula 4, in the case of when B of X is the hetero ringgroup, it is preferable that B is the thiophenyl group, the imidazolegroup, the oxazol group, the pyridyl group, the triazynyl group, thequinolynyl group, the isoquinolynyl group, and the carbazolyl group.

In Formula 1 to Formula 4, the preferable compounds as the holeinjection layer are materials that have substituents having the HOMOvalues capable of being smaller than that of the hole transport layer.That is, it allows the carrier to easily move from ITO (indium tinoxide) to the hole transport layer, and as these substituents, materialsthat comprise the arylamino group, the arylaminoaryl group, or thethiophenyl group and the like are preferable. In addition, among thepositions at which they can be substituted with X and R¹ to R⁸, R¹ to R⁸are preferable.

In Formula 1 to Formula 4, it is preferable that the substituent group Xis selected from the substituent groups described in the following TableA-1, but it is not limited thereto.

TABLE A-1

In Formula 1 to Formula 4, it is preferable that the substituent groupY1 is selected from the substituent groups described in the followingTable Y-A-1, but it is not limited thereto.

TABLE Y-1 —Y1

The Structural Formulas of the following figures A-1 to A-6 can besubstituted by the substituent groups of Table A-1 and Table Y-1.

As shown in figures A-1 to A-6, L1 to L2 of Formula 1 to Formula 3 canbe substituted by the aryl group, the heteroaryl group, the arylaminogroup and the like, and it is preferable that Y1 to Y2 are the arylaminogroup, the heteroarylamino group, the aralkylamino group or thecarbazolyl group.

In addition, the present invention provides a method for manufacturingthe derivative that is represented by Formula 1. The method formanufacturing the compound according to the present invention isdisclosed in the document [Journal of Tetrahedron 2005, 61, 1681-1691],and the compounds A and B are manufactured like the following ReactionEquation 1 according to the method disclosed in the above document, butthe method for manufacturing the derivative that is represented byFormula 1 is not limited to the following Reaction Equation 1.

In Reaction Equation 1, X, and R¹ to R⁸ are the same as R¹ to R⁸ definedby Formula 1.

The method for manufacturing the compound of Formula 1 according to thepresent invention introduces X of Formula A manufactured in the aboveEquation under the Pd catalyst, introduces the bromo group with NBS orBr₂, and introduces the substituent group R³ under the Pd catalyst tomanufacture Formula 1.

The compound of Formula 1 is characterized in that it has a corestructure in which at least one benzene ring is condensated in thecarbazole structure.

The conjugation length of the compound has a close relationship with anenergy band gap. In detail, the energy band gap is reduced as theconjugation length of the compound increases. As described above, sincea conjugation structure is limited in the core structure of the compoundof Formula 1, the core structure has a large energy band gap.

As described above, in the present invention, various substituent groupsare introduced to L1, L2, X, Y1, or Y2 positions of the core structurehaving the large energy band gap so as to produce compounds havingvarious energy band gaps. Generally, it is easy to control an energyband gap by introducing substituent groups into a core structure havinga large energy band gap, but it is difficult to significantly controlthe energy band gap by introducing substituent groups into a corestructure having a small energy band gap. Furthermore, in the presentinvention, it is possible to control HOMO and LUMO energy levels of thecompound by introducing various substituent groups into L, X, or Y ofthe core structure.

Additionally, by introducing various substituent groups into the corestructure, compounds having intrinsic characteristics of the substituentgroups may be obtained. For example, substituent groups, which arefrequently applied to hole injection layer material, hole transportlayer material, light emitting layer material, and electron transportlayer materials during the production of the organic light emittingdevice and the organic electronic device, are introduced into the corestructure so as to produce substances capable of satisfying therequirements of each organic material layer. For example, the arylaminogroup, the thiophenyl group or the aryl group that is substituted withthem may be introduced. Formula 1 in which the arylamino group or thethiophenyl group is introduced shows HOMO characteristic that is in therange of 5.6 to 5.1 eV, and it is very useful to use as the holeinjection and hole transport layer.

Furthermore, various substituent groups are introduced into the corestructure so as to precisely control the energy band gap, and to improveinterfacial characteristics with organic material layers, thereby applythe compound to various fields.

In addition, by controlling the number of amine that is comprised in thesubstituent group B, it is possible to finely control HOMO and LUMOenergy level and energy band gap, improve interfacial characteristicswith organic materials, and make the purpose of material various.

In addition, if an appropriate substituent is introduced to thestructure of Formula 1, energy band gap and stability can be ensured ata triplet state. From these results, various phosphorescence dopantsfrom red color to blue color can be used and applied to light emittinglayers of fluorescent and phosphorescent devices.

In addition, since the compound of Formula 1 has a high glass transitiontemperature (Tg), it has excellent thermal stability. Such increase inthermal stability is an important factor providing driving stability tothe device.

Furthermore, the compound of Formula 1 may be used to form the organicmaterial layer using a vacuum deposition process or a solution coatingprocess during the production of the organic light emitting device. Inconnection with this, illustrative, but non-limiting, examples of thesolution coating process comprise a spin coating process, a dip coatingprocess, an inkjet printing process, a screen printing process, a sprayprocess, and a roll coating process.

The organic electronic device of the present invention may be producedusing known materials through a known process, modified only in that atleast one layer of organic material layer(s) comprise the compound ofthe present invention, that is, the compound of Formula 1. A compoundaccording to the present invention may be used as a hole injectionmaterial, a hole transport material, a light emitting material, anelectron transport material, an electron injection material and thelike, and it is more preferable that it is used as a hole injectionmaterial and a hole transport material in an organic electronic deviceaccording to the present invention. In addition, on the basis of theapplication of the compound according to the present invention to theorganic light emitting device, those who are skilled in the art can usethe compound according to the present invention in other organicelectronic devices. The organic electronic device according to thepresent invention comprises an organic light emitting device, an organicphosphorescent device, an organic solar cell, an organic photoconductorand an organic transistor.

The organic material layer(s) of the organic electronic device accordingto the present invention may have a single layer structure, oralternatively, a multilayered structure in which at least two organicmaterial layers are layered. For example, the organic light emittingdevice of the present invention may comprise a hole injection layer, ahole transport layer, a light emitting layer, an electron transportlayer, and an electron injection layer as the organic material layer(s).However, the structure of the organic light emitting device is notlimited to this, but may comprise a smaller number of organic materiallayers. The structure of the organic light emitting device according tothe present invention is illustrated in FIGS. 1 and 2, but is notlimited thereto.

Furthermore, the organic light emitting device of the present inventionmay be produced, for example, by sequentially layering a firstelectrode, organic material layer(s), and a second electrode on asubstrate. In connection with this, a physical vapor deposition (PVD)method, such as a sputtering method or an e-beam evaporation method, maybe used, but the method is not limited to these.

MODE FOR INVENTION

The method for manufacturing the compound of Formula 1 and themanufacturing of an organic light emitting device using the same will bedescribed in detail in Preparation Examples and Examples. However, thefollowing Preparation Examples and Examples are set forth to illustratethe present invention, but the scope of the present invention is notlimited thereto.

The compound of Formula 1 according to the present invention can bemanufactured with multistage chemical reactions. The manufacturing ofthe compounds is described in the following Synthesis Examples andPreparation Examples. As described in the following Synthesis Examples,some intermediate compounds are first manufactured, and as described inPreparation Examples, the compounds of Formula 1 are manufactured fromthe intermediate compounds.

The compounds of Formula 1 can be manufactured by using the same methodand order as the following Reaction Equations 1-1, 1-2, and 1-3, but thereaction is not limited thereto and the Reaction Equations are simplydescribed for convenience of understanding. As shown by the ReactionEquation 1-1, various tetralone compounds can be deformed as the centralcore of the present Formula. These reactions can be easily performed bythe known manufacturing method of Reaction Equation 1.

The central cores manufactured by Reaction Equation 1-1 can beintroduced with various substituents through suzuki coupling orbromination like Reaction Equations 1-2 and 1-3, and with thesubstituent groups such as the aryl group, the heteroaryl group, and thearylamino group under the Pd catalyst.

In order to manufacture the compound of Formula 1, agents andintermediates described in Table 1-1 are required, and these are easilyobtained on the market and manufactured by using a known method.

The following Synthesis Examples are intermediated compounds tomanufacture the compound of Formula 1.

TABLE 1-1

compound S-1

compound S-2

compound S-3

compound S-4

compound S-5

compound S-6

compound S-7

compound S-8

compound S-9

compound S-10

compound S-11

compound S-12

compound S-13

compound S-14

compound S-15

compound S-16

compound S-17

compound S-18

compound S-19

compound S-20

compound S-21

compound S-22

compound S-23

compound S-24

compound S-25

compound S-26

compound S-27

compound S-28

compound S-29

compound S-30

compound S-31

compound S-32

compound S-33

compound S-34

compound S-35

compound S-36

compound S-37

compound S-38

compound S-39

compound S-40

compound S-41

compound S-42

compound S-43

compound S-44

compound S-45

The compounds of Formula 1 are manufactured according to the followingexamples, but are not limited thereto. The following Synthesis Examplesare Synthesis Examples of the intermediate compound to manufacture thecompound of Equation 1.

TABLE 2-1 Synthesis Example yield 1-1-No compound R6 (%) MS 1-1-1compound 1-A Br 86 [M]+ = 298 1-1-2 compound 1-B Br 96 [M]+ = 296

1-1-1. Manufacturing of the Compound 1-A

a-Tetralone (21.6 g, 148 mmol), and 4-bromophenylhydrazine chloride(20.4 g, 91 mmol) were put into a small amount of acetic acid, andrefluxed in 300 mL of ethanol for 2 hours under nitrogen atmosphere.After they were cooled to normal temperature, the formed product wasfiltered and dried to manufacture the compound 1-A (19.6 g, yield 86%).

MS: [M]⁺=298

1-1-2. Manufacturing of the Compound 1-B

The compound 1-A (24.1 g, 80.5 mmol), and tetrachloro-1,4-benzoquinone(27.45 g, 111.7 mmol) were refluxed under the nitrogen atmosphere in 300ml of xylene for 2 hours. NaOH (10%) and water were put into thereaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 1-B (22.9 g, yield96%).

MS: [M]⁺=296

TABLE 1-B-No Synthesis Example compound 1-B-No 1-B-No R6 X yield(%) MS1-B-1 compound 1-B-1 Br

76 [M]+ = 372

Synthesis Example 1-B-No Manufacturing of the Compound Represented byFormula 1-B-No

The compound 1-B, the aryl compound that was substituted with anexcessive amount of iodine, 1 to 2 equivalents of Cu powder, and 3 to 6equivalents of K₂CO₃ was added thereto, heated and agitated. Thereactants were cooled to normal temperature, and extracted, distilled,purified, and dried with the organic solvent to manufacture the 1-B-Nocompound, the specific compound synthesized 1-B-1, and the resultsthereof are described in Table 1-B-No.

Synthesis Example 1-B-1 Manufacturing of the Compound Represented byFormula 1-B-1

The compound 1-B (10.0 g, 33.8 mmol), 120 ml of iodobenzene, 2equivalents of Cu powder (4.3 g, 67.6 mmol), and 3 equivalents of K₂CO₃(14.0 g, 101.4 mmol) were added thereto, heated and agitated for 12hours. The reactants were cooled to normal temperature, extracted anddistilled with the organic solvent, subjected to the columnchromatography purification using n-hexane as the developing solvent,and dried to manufacture the 1-B-1 compound (22.9 g, yield 76%).

TABLE 3-1 Synthesis Example compound yield 1-1-No 1B-No —L1—Y0 (%) MS1-1-3 compound 1B-1

58 [M]+ = 327 1-1-4 compound 1B-2

62 [M]+ = 403 1-1-5 compound 1B-3

76 [M]+ = 409

Synthesis Example 1-1-No Synthesis of the Compound 1B-No

The compound 1-B, and 1 to 1.5 equivalents of the substituted orunsubstituted arylboronic acid (or arylboron ester) or substituted orunsubstituted heteroarylboronic acid (or arylboron ester) were put,dissolved in THF, 0.02 equivalents of Pd(PPh₃) and 2 equivalents or moreof 2M K₂CO₃/H₂O aqueous solution were added, and heated and agitated for3 to 16 hours. The reaction mixture was cooled to normal temperature,filtered or extracted with the organic solvent, separated, purified, anddried to manufacture the 1-B-No compound, and the results thereof aredescribed in Table 3-1.

1-1-3. Manufacturing of the Compound 1B-1

After the compound 1-B (4.48 g, 15.13 mmol) and 4-chlorophenyl boronicacid (2.84 g, 18.15 mmol) were dissolved in THF (150 mL), Pd(PPh₃)₄(0.52 g, 0.45 mmol) and 70 ml of 2M K₂CO₃/H₂O aqueous solution were putthereinto and refluxed for 3 hours. Distilled water was put into thereaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 1B-1 (2.88 g, yield58%).

1-1-4. Manufacturing of Formula 1B-2

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 1B-2(3.79 g, yield 62%), except that 4-(4-chlorophenyl)phenyl boronic acid(4.22 g, 18.15 mmol) was used instead of 4-chlorophenyl boronic acid.

1-1-5. Manufacturing of the Compound 1B-3

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 1B-3(4.71 g, yield 76%), except that 5-(4-chlorophenyl)thiophenyl-2-boronicacid (4.33 g, 18.15 mmol) was used instead of 4-chlorophenyl boronicacid.

TABLE 4-1 Synthesis Example yield 1-2-No 1C-No X —L1—Y0 (%) MS 1-2-1compound 1C-1

65 [M]+ = 403 1-2-2 compound 1C-2

69 [M]+ = 479 1-2-3 compound 1C-3

58 [M]+ = 485 1-2-4 compound 1C-4

31 [M]+ = 595 1-2-5 compound 1C-5

43 [M]+ = 479 1-2-6 compound 1C-6

58 [M]+ = 555 1-2-7 compound 1C-7

48 [M]+ = 561 1-2-8 compound 1C-8

61 [M]+ = 561 1-2-9 compound 1C-9

76 [M]+ = 561 1-2-10 compound 1C-10

89 [M]+ = 408 1-2-11 compound 1C-11

82 [M]+ = 421 1-2-12 compound 1C-12

43 [M]+ = 558 1-2-13 compound 1C-13

73 [M]+ = 634

Synthesis Example 1-2-No Synthesis of the Compound 1C-No

The compound 1B-No and 1 to 1.4 equivalents of substituted orunsubstituted aryl halide or substituted or unsubstituted heterohalidewere put, dissolved in xylene or toluene, and 1.4 to 2 equivalents ofsodium-tertiary-botoxide and 0.01 to 0.06 equivalents of Pd[P(t-Bu)₃]₂were added thereto, and heated and agitated for 5 to 12 hours. Thereactants were cooled to normal temperature, filtered or extracted withthe organic solvent, separated, purified, and dried to manufacture the1B-No compound.

1-2-1. Manufacturing of the Compound 1C-1

The compound 1B-1 (12.65 g, 38.6 mmol), and bromobenzene (7.3 g, 46.3mmol) were dissolved in 200 ml of xylene, sodium-tertiary-botoxide (5.6g, 57.9 mmol), and 0.19 g of Pd[P(t-Bu)₃]₂ (0.386 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=10/1 solvent, it was agitated inpetroleum ether, and dried under vacuum to manufacture the compound 1C-1(10.19 g, yield 65%).

1-2-2. Manufacturing of the Compound 1C-2

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-2(12.78 g, yield 69%), except that the compound 1B-2 (15.59 g, 38.6 mmol)was used instead of the compound 1B-1.

1-2-3. Manufacturing of the Compound 1C-3

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-3(10.88 g, yield 58%), except that the compound 1B-3 (15.82 g, 38.6 mmol)was used instead of the compound 1B-1.

1-2-4. Manufacturing of the Compound 1C-4

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-5(3.66 g, yield 31%), except that the compound S-21 (6.98 g, 20.0 mmol)was used instead of the compound 1B-1 (6.55 g, 20.0 mmol) andbromobenzene.

1-2-5. Manufacturing of the Compound 1C-5

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-5(7.97 g, yield 43%), except that iodobiphenyl (12.96 g, 46.3 mmol) wasused instead of the compound 1B-1 (12.65 g, 38.6 mmol) and bromobenzene.

1-2-6. Manufacturing of the Compound 1C-6

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-6(12.45 g, yield 58%), except that iodobiphenyl (12.96 g, 46.3 mmol) wasused instead of the bromobenzene, and the compound 1B-2 (15.59 g, 38.6mmol) was used instead of the compound 1B-1.

1-2-7. Manufacturing of the Compound 1C-7

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-7 (7.6g, yield 48%), except that iodobiphenyl (12.96 g, 46.3 mmol) usedinstead of the bromobenzene, and the compound 1B-3 (15.82 g, 38.6 mmol)was used instead of the compound 1B-1.

1-2-8. Manufacturing of the Compound 1C-8

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-8(13.23 g, yield 61%), except that the compound S-14 (12.96 g, 46.3 mmol)was used instead of the compound 1B-1 (12.65 g, 38.65 mmol) andbromobenzene.

1-2-9. Manufacturing of the Compound 1C-9

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-9(16.49 g, yield 76%), except that the compound S-15 (12.96 g, 46.3 mmol)was used instead of the compound 1B-1 (12.65 g, 38.6 mmol) andbromobenzene.

1-2-10. Manufacturing of the Compound 1C-10

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-10(5.46 g, yield 89%), except that the compound S-20 (2.75 g, 17.0 mmol)was used instead of the compound 1B-1 (4.92 g, 15.0 mmol) andbromobenzene.

1-2-11. Manufacturing of the Compound 1C-11

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-10(4.87 g, yield 77%), except that the compound S-22 (2.98 g, 17.0 mmol)was used instead of the compound 1B-1 (4.92 g, 15.0 mmol) andbromobenzene.

1-2-12. Manufacturing of the Compound 1C-12

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-12(10.4 g, yield 62%), except that the compound S-18 (8.01 g, 32.0 mmol)was used instead of the compound 1B-1 (9.83 g, 30.0 mmol) andbromobenzene.

1-2-13. Manufacturing of the Compound 1C-13

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 1C-12(11.05 g, yield 87%), except that the compound S-23 (7.56 g, 22.0 mmol)was used instead of the compound 1B-1 (6.55 g, 20.0 mmol) andbromobenzene.

TABLE 5-1 Synthesis Example 2-1-No compound R6 MS 2-1-1 compound 2-A H[M + H]+ = 220 2-1-2 compound 2-B H [M + H]+ = 218

2-1-1. Manufacturing of the Compound 2-A

In Synthesis Example 1-1-1, it was synthesized in the same method tomanufacture the compound 2-A, except that phenylhydrazine chloride wasused instead of 4-bromophenylhydrazine chloride.

2-1-2. Manufacturing of the Compound 2B-1

In Synthesis Example 1-1-2, it was synthesized in the same method tomanufacture the compound 2-B, except that the compound 2-A that wasmanufactured in Synthesis Example 2-1-1 was used instead of the compound1A-1.

TABLE 6-1 Synthesis Example compound 2-1-No 2B-No —X MS 2-1-3 compound2B-1

[M + H]+ = 294 2-1-4 compound 2B-2

[M + H]+ = 370 2-1-5 compound 2B-3

[M + H]+ = 452 2-1-6 compound 2B-4

[M + H]+ = 299 2-1-7 compound 2B-5

[M + H]+ = 312 2-1-8 compound 2B-6

[M + H]+ = 525

Synthesis Example 2-1-No Synthesis of the Compound 2B-No

The compound 2-B and 1 to 1.4 equivalents of substituted orunsubstituted aryl halide or substituted or unsubstituted heterohalidewere put, dissolved in xylene or toluene, and 1.4 to 2 equivalents ofsodium-tertiary-botoxide and 0.01 equivalents of Pd[P(t-Bu)₃]₂ wereadded thereto, and heated and agitated for 5 to 12 hours. The reactantswere cooled to normal temperature, filtered or extracted with theorganic solvent, separated, purified, and dried to manufacture the 2B-Nocompound.

2-1-3. Manufacturing of the Compound 2B-1

In the manufacturing of the compound 1C-1 of Synthesis Example 1-2-1, itwas synthesized in the same method to manufacture the compound 2B-1,except that the compound 2-B was used instead of the compound 1B-1.

2-1-4. Manufacturing of the Compound 2B-2

In the manufacturing of the compound 1C-5 of Synthesis Example 1-2-4, itwas synthesized in the same method to manufacture the compound 2B-2,except that the compound 2-B was used instead of the compound 1B-1.

2-1-5. Manufacturing of the Compound 2B-3

In the manufacturing of the compound 1C-8 of Synthesis Example 1-2-9, itwas synthesized in the same method to manufacture the compound 2B-3,except that the compound 2-B was used instead of the compound 1B-1.

2-1-6. Manufacturing of the Compound 2B-4

In the manufacturing of the compound 1C-10 of Synthesis Example 1-2-10,it was synthesized in the same method to manufacture the compound 2B-4,except that the compound 2-B was used instead of the compound 1B-1.

2-1-7. Manufacturing of the Compound 2B-5

In the manufacturing of the compound 1C-11 of Synthesis Example 1-2-11,it was synthesized in the same method to manufacture the compound 2B-5,except that the compound 2-B was used instead of the compound 1B-1.

2-1-8. Manufacturing of the Compound 2B-6

In the manufacturing of the compound 1C-13 of Synthesis Example 1-2-13,it was synthesized in the same method to manufacture the compound 2B-6,except that the compound 2-B was used instead of the compound 1B-1.

TABLE 7-1 Syn- thesis Ex- ample 2-2- No 2C-No —X MS 2-2-1 com- pound2C-1

[M]+ = 372 2-2-2 com- pound 2C-2

[M]+ = 448 2-2-3 com- pound 2C-3

[M]+ = 530 2-2-4 com- pound 2C-4

[M]+ = 377 2-2-5 com- pound 2C-5

[M]+ = 390 2-2-6 com- pound 2C-6

[M]+ = 603

Synthesis Example 2-2-No Synthesis of the Compound 2C-No

The compound 2B-No was dissolved in chloroform, and 1 equivalent ofN-bromo succinimide was added thereto, and agitated for 3 to 8 hours atnormal temperature. Distilled water was put into the reaction solution,the termination of the reaction was carried out, and the organic layerwas extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 2C-No.

2-2-1. Manufacturing of the Compound 2C-1

The compound 2B-1 (3.57 g, 12.18 mmol) was dissolved in chloroform (120mL), and N-bromo succinimide (2.17 g, 12.18 mmol) was added thereto, andagitated for 5 hours at normal temperature. Distilled water was put intothe reaction solution, the termination of the reaction was carried out,and the organic layer was extracted. The reaction solution wasconcentrated, and recrystallized with EtOH to manufacture the compound2C-1 (4.12 g, yield 91%).

2-2-2. Manufacturing of the Compound 2C-2

In the manufacturing of the compound 2C-1 of Synthesis Example 2-2-1, itwas synthesized in the same method to manufacture the compound 2C-2,except that the compound 2B-2 was used instead of the compound 2B-1.

2-2-3. Manufacturing of the Compound 2C-3

In the manufacturing of the compound 2C-1 of Synthesis Example 2-2-1, itwas synthesized in the same method to manufacture the compound 2C-3,except that the compound 2B-3 was used instead of the compound 2B-1.

2-2-4. Manufacturing of the Compound 2C-4

In the manufacturing of the compound 2C-1 of Synthesis Example 2-2-1, itwas synthesized in the same method to manufacture the compound 2C-4,except that the compound 2B-4 was used instead of the compound 2B-1.

2-2-5. Manufacturing of the Compound 2C-5

In the manufacturing of the compound 2C-1 of Synthesis Example 2-2-1, itwas synthesized in the same method to manufacture the compound 2C-5,except that the compound 2B-5 was used instead of the compound 2B-1.

2-2-6. Manufacturing of the Compound 2C-6

In the manufacturing of the compound 2C-1 of Synthesis Example 2-2-1, itwas synthesized in the same method to manufacture the compound 2C-6,except that the compound 2B-6 was used instead of the compound 2B-1.

TABLE 8-1 Synthesis compound Example 2D-No/ 2-3-No (reactant) —X —L1—Y0MS 2-3-1 compound 2D-1/ (2C-1)

[M]+ = 403 2-3-2 compound 2D-2/ (2C-1)

[M]+ = 479 2-3-3 compound 2D-3/ (2C-1)

[M]+ = 485 2-3-4 compound 2D-4/ (2C-1)

[M]+ = 370 2-3-5 compound 2D-5/ (2C-2)

[M]+ = 479 2-3-6 compound 2D-6/ (2C-2)

[M]+ = 555 2-3-7 compound 2D-7/ (2C-7)

[M]+ = 561 2-3-8 compound 2D-8/ (2C-3)

[M]+ = 561 2-3-9 compound 2D-9/ (2C-4)

[M]+ = 408 2-3-10 compound 2D-10/ (2C-5)

[M]+ = 421 2-3-11 compound 2D-11/ (2C-6)

[M]+ = 634 2-3-12 compound 2D-12/ (2C-2)

[M]+ = 446

Synthesis Example 2-3-No Synthesis of the Compound 2D-No

The compound 2C-No, and 1 to 1.5 equivalents of arylboronic acid (orboron ester) or the substituted or unsubstituted heteroarylboronic acid(or boron ester) were put, dissolved in THF, 0.02 equivalents ofPd(PPh₃) and 2 equivalents or more of 2M K₂CO₃/H₂O aqueous solution wereadded, and heated and agitated for 3 to 16 hours. The reaction mixturewas cooled to normal temperature, filtered or extracted with the organicsolvent, separated, purified, and dried to manufacture the 2D-Nocompound.

2-3-1. Manufacturing of the Compound 2D-1

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2D-1,except that the compound 2C-1 was used instead of the compound 1-B.

2-3-2. Manufacturing of the Compound 2D-2

In the manufacturing of the compound 1B-2 of Synthesis Example 1-1-4, itwas synthesized in the same method to manufacture the compound 2D-2,except that the compound 2C-1 was used instead of the compound 1-B.

2-3-3. Manufacturing of the Compound 2D-3

In the manufacturing of the compound 1B-3 of Synthesis Example 1-1-5, itwas synthesized in the same method to manufacture the compound 2D-3,except that the compound 2C-1 was used instead of the compound 1-B.

2-3-4. Manufacturing of the Compound 2D-4

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2D-4,except that the compound 2C-1 was used instead of the compound 1-B andphenyl boronic acid was used instead of 4-chlorophenyl boronic acid.

2-3-5. Manufacturing of the Compound 2D-5

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2D-5,except that the compound 2C-2 was used instead of the compound 1-B.

2-3-6. Manufacturing of the Compound 2D-6

In the manufacturing of the compound 1B-2 of Synthesis Example 1-1-4, itwas synthesized in the same method to manufacture the compound 2D-6,except that the compound 2C-2 was used instead of the compound 1-B.

2-3-7. Manufacturing of the Compound 2D-7

In the manufacturing of the compound 1B-3 of Synthesis Example 1-1-5, itwas synthesized in the same method to manufacture the compound 2D-7,except that the compound 2C-2 was used instead of the compound 1-B.

2-3-8. Manufacturing of the Compound 2D-8

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2D-8,except that the compound 2C-3 was used instead of the compound 1-B.

2-3-9. Manufacturing of the Compound 2D-9

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2D-9,except that the compound 2C-4 was used instead of the compound 1-B.

2-3-10. Manufacturing of the Compound 2D-10

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2D-10,except that the compound 2C-5 was used instead of the compound 1-B.

2-3-11. Manufacturing of the Compound 2D-11

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2D-11,except that the compound 2C-6 was used instead of the compound 1-B.

2-3-12. Manufacturing of the Compound 2D-12

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2D-12,except that the compound 2C-2 was used instead of the compound 1-B.

TABLE 9-1 Synthesis Example 2E-No 2-4-No (reactant) —X —L1—Y0 MS 2-4-1compound 2E-1 (2D-1)

[M]+ = 482 2-4-2 compound 2E-2 (2D-5)

[M]+ = 558 2-4-3 compound 2E-3 (2D-4)

[M]+ = 448 2-4-4 compound 2E-4 (2D-8)

[M]+ = 640 2-4-5 compound 2E-5 (2D-9)

[M]+ = 487 2-4-6 compound 2E-6 (2D-10)

[M]+ = 500 2-4-7 compound 2E-7 (2D-11)

[M]+ = 713 2-4-8 compound 2E-8 (2D-12)

[M]+ = 524

Synthesis Example 2-4-No Synthesis of the compound 2E-No

In the manufacturing of the compound 2C-1 of Synthesis Example 2-2-1, itwas synthesized in the same method to manufacture the compound 2E-1,compound 2E-2, compound 2E-3, compound 2E-4, compound 2E-5, compound2E-6, compound 2E-7, and compound 2E-8, except that the compound 2D-1,compound 2D-5, compound 2D-4, compound 2D-8, compound 2D-9, compound2D-10, compound 2D-11, and compound 2D-12 were used instead of thecompound 2B-1.

TABLE 10-1 Synthesis compound Example 2F-No 2-5-No (reactant) X —L1—Y0—L2—Y0 MS 2-5-1 compound 2F-1 (2E-1)

[M]+ = 479 2-5-2 compound 2F-2 (2E-2)

[M]+ = 631 2-5-3 compound 2F-3 (2E-3)

[M]+ = 479 2-5-4 compound 2F-4 (2E-4)

[M]+ = 795 2-5-5 compound 2F-5 (2E-1)

[M]+ = 513 2-5-6 compound 2F-6 (2E-5)

[M]+ = 484 2-5-7 compound 2F-7 (2E-6)

[M]+ = 664 2-5-8 compound 2F-8 (2E-7)

[M]+ = 710 2-5-9 compound 2F-9 (2E-1)

[M]+ = 595 2-5-10 compound 2F-10 (2E-8)

[M]+ = 556

Synthesis Example 2-5-No Synthesis of the Compound 2F-No

The compound 2E-No, and 1 to 1.5 equivalents of arylboronic acid (orboron ester) or the substituted or unsubstituted heteroarylboronic acid(or boron ester) were put, dissolved in THF, 0.02 equivalents ofPd(PPh₃) and 2 equivalents or more of 2M K₂CO₃/H₂O aqueous solution wereadded, and heated and agitated for 3 to 16 hours. The reaction mixturewas cooled to normal temperature, filtered or extracted with the organicsolvent, separated, purified, and dried to manufacture the 2F-Nocompound.

2-5-1. Manufacturing of the Compound 2F-1

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-1,except that the compound 2E-1 was used instead of the compound 1-B andphenyl boronic acid was used instead of 4-chlorophenyl boronic acid.

2-5-2. Manufacturing of the Compound 2F-2

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-2,except that the compound 2E-2 was used instead of the compound 1-B andbiphenyl boronic acid was used instead of 4-chlorophenyl boronic acid.

2-5-3. Manufacturing of the Compound 2F-3

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-3,except that the compound 2E-3 was used instead of the compound 1-B.

2-5-4. Manufacturing of the Compound 2F-4

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-4,except that the compound 2E-4 was used instead of the compound 1-B andthe compound S-10 was used instead of 4-chlorophenyl boronic acid.

2-5-5. Manufacturing of the Compound 2F-5

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-5,except that the compound 2E-1 was used instead of the compound 1-B.

2-5-6. Manufacturing of the Compound 2F-6

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-6,except that the compound 2E-5 was used instead of the compound 1-B andphenyl boronic acid was used instead of 4-chlorophenyl boronic acid.

2-5-7. Manufacturing of the Compound 2F-7

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-7,except that the compound 2E-6 was used instead of the compound 1-B andthe compound S-8 was used instead of 4-chlorophenyl boronic acid.

2-5-8. Manufacturing of the Compound 2F-8

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-8,except that the compound 2E-7 was used instead of the compound 1-B andphenyl boronic acid was used instead of 4-chlorophenyl boronic acid.

2-5-9. Manufacturing of the Compound 2F-9

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-9,except that the compound 2E-1 was used instead of the compound 1-B andthe compound S-19 was used instead of 4-chlorophenyl boronic acid.

2-5-10. Manufacturing of the Compound 2F-10

In the manufacturing of the compound 1B-1 of Synthesis Example 1-1-3, itwas synthesized in the same method to manufacture the compound 2F-10,except that the compound 2E-8 was used instead of the compound 1-B.

TABLE 11-1 Synthesis Example yield 3-1-No compound X (%) MS 3-1-1compound 3-A 64 [M + H]+ = 250 3-1-2 compound 3-B-1 67 [M + H]+ = 2483-1-3 compound 3-B-2

90 [M + H]+ = 324 3-1-4 compound 3-B-3

92 [M + H]+ = 310 3-1-5 compound 3-B

90 [M + H]+ = 426 3-1-6 compound 4-B-2

78 [M + H]+ = 340 3-1-7 compound 4-B-3

92 [M + H]+ = 386 3-1-8 compound 4-B

90 [M + H]+ = 502

3-1-1. Manufacturing of the Compound 3-A

6-methoxy-1-tetralone (17.6 g, 100 mmol), and phenylhydrazinehydrochloride (11 g, 76 mmol) were added to a small amount of aceticacid and 150 ml of ethanol, and refluxed for 2 hours under the nitrogenatmosphere. After they were cooled to normal temperature, the formedproduct was filtered and dried to manufacture the compound 3-A (15.88 g,yield 64%).

3-1-2. Manufacturing of the Compound 3-B-1

The compound 3-A (15.88 g, 63.69 mmol), and tetrachloro-1,4-benzoquinone(21.92 g, 89.17 mmol) were refluxed under the nitrogen atmosphere in 300ml of xylene for 2 hours. NaOH (10%) and water were put into thereaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 3-B-1 (10.5 g,yield 67%).

3-1-3. Manufacturing of the Compound 3-B-2

The compound 3-B-1 (5 g, 20.22 mmol), and bromobenzene (3.8 g, 24.26mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (2.9g, 30.33 mmol), and Pd[P(t-Bu)₃]₂ (0.10 g, 0.20 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=10/1 solvent, it was agitated inpetroleum ether, and dried under vacuum to manufacture the compound3-B-2 (5.88 g, yield 90%).

3-1-4. Manufacturing of the Compound 3-B-3

The compound 3-B-2 (5.1 g, 15.77 mmol) and pyridine hydrochloride (10.93g, 94.62 mmol) were heated and agitated for 40 min. After the reactionwas finished, it was cooled to normal temperature, the precipitate thatwas obtained by adding 300 ml of water was filtered and dried tomanufacture the compound 3-B-3 (4.5 g, yield 92%).

3-1-5. Manufacturing of the Compound 3-B

The compound 3-B-3 (4.5 g, 14.54 mmol), and pyridine (12 ml, 29.08 mmol)were agitated 150 ml of methylene chloride, and at 0° C.trifluoromethanesulfonic anhydride (18 ml, 21.81 mmol) was slowly putthereinto. The reaction temperature was increased to normal temperatureand it was agitated for 24 hours. After the reaction was finished, theprecipitate that was obtained by adding 200 ml of water was filtered anddried to manufacture the compound 3-B (5.1 g, yield 82%).

3-1-6. Manufacturing of the Compound 4-B-2

The compound 3-B-1 (5 g, 20.22 mmol), and bromobiphenyl (5.65 g, 24.26mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (2.9g, 30.33 mmol), and Pd[P(t-Bu)₃]₂ (0.10 g, 0.20 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=10/1 solvent, it was agitated inpetroleum ether, and dried under vacuum to manufacture the compound4-B-2 (6.3 g, yield 78%).

3-1-7. Manufacturing of the Compound 4-B-3

The compound 4-B-2 (6.3 g, 15.77 mmol) and pyridine hydrochloride (10.93g, 94.62 mmol) were heated and agitated for 40 min. After the reactionwas finished, it was cooled to normal temperature, the precipitate thatwas obtained by adding 300 ml of water was filtered and dried tomanufacture the compound 4-B-3 (5.6 g, yield 92%).

3-1-8. Manufacturing of the Compound 4-B

The compound 4-B-3 (5.6 g, 14.54 mmol), and pyridine (12 ml, 29.08 mmol)were agitated 150 ml of methylene chloride, and at 0° C.trifluoromethanesulfonic anhydride (18 ml, 21.81 mmol) was slowly putthereinto. The reaction temperature was increased to normal temperatureand it was agitated for 24 hours. After the reaction was finished, theprecipitate that was obtained by adding 200 ml of water was filtered anddried to manufacture the compound 4-B (6.1 g, yield 83.6%).

TABLE 12-1 Synthesis compound Example 3B-No 3-2-No (reactant) —X —L1—Y0MS 3-2-1 compound 3B-1 (3-B)

[M + H]+ = 370 3-2-2 compound 3B-2 (3-B)

[M]+ = 403 3-2-3 compound 3B-3 (3-B)

[M + H]+ = 446 3-2-4 compound 3B-4 (4-B)

[M + H]+ = 446 3-2-5 compound 3B-5 (4-B)

[M]+ = 479

Synthesis Example 3-2-No Synthesis of the Compound 3B-No

The compound No-B, and 1 to 1.5 equivalents of the substituted orunsubstituted arylboronic acid (or boron ester) or substituted orunsubstituted heteroarylboronic acid (or boron ester) were put,dissolved in THF, 0.02 equivalents of Pd(PPh₃) and 2 equivalents or moreof 2M K₂CO₃/H₂O aqueous solution were added, and heated and agitated for3 to 16 hours. The reaction mixture was cooled to normal temperature,filtered or extracted with the organic solvent, separated, purified, anddried to manufacture the 3B-No compound.

3-2-1. Manufacturing of the Compound 3B-1

After the compound 3-B (5.1 g, 11.99 mmol) and phenyl boronic acid (1.76g, 14.47 mmol) were dissolved in THF (150 mL), Pd(PPh₃)₄ (0.46 g, 0.39mmol) and 70 ml of 2M K₂CO₃/H₂O aqueous solution were put thereinto andrefluxed for 3 hours. Distilled water was put into the reactionsolution, the termination was carried out, and the organic layer wasextracted. The reaction solution was concentrated, and recrystallizedwith EtOH to manufacture the compound 3B-1 (4.1 g, yield 93%).

3-2-2. Manufacturing of the Compound 3B-2

After the compound 3-B (5.6 g, 13.16 mmol) and 4-chlorophenyl boronicacid (2.27 g, 14.47 mmol) were dissolved in THF (150 mL), Pd(PPh₃)₄(0.46 g, 0.39 mmol) and 70 ml of 2M K₂CO₃/H₂O aqueous solution were putthereinto and refluxed for 3 hours. Distilled water was put into thereaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 3B-2 (4.68 g, yield88%).

3-2-3. Manufacturing of the Compound 3B-3

In the manufacturing of the compound 3B-1 of Synthesis Example 3-2-1, itwas synthesized in the same method to manufacture the compound 3B-3,except that the compound biphenylboronic acid was used instead ofphenylboronic acid.

3-2-4. Manufacturing of the Compound 3B-4

In the manufacturing of the compound 3B-1 of Synthesis Example 3-2-1, itwas synthesized in the same method to manufacture the compound 3B-4,except that the compound 4-B was used instead of the compound 3-B.

3-2-5. Manufacturing of the Compound 3B-5

In the manufacturing of the compound 3B-1 of Synthesis Example 3-2-1, itwas synthesized in the same method to manufacture the compound 3B-5,except that the compound 4-B was used instead of the compound 3-B and4-chlorophenyl boronic acid was used instead of phenyl boronic acid.

TABLE 13-1 Synthesis compound Example 3C-No 3-3-No (reactant) —X —L1—Y0MS 3-3-1 compound 3C-1 (3B-1)

[M]+ = 448 3-3-2 compound 3C-2 (3B-2)

[M]+ = 524 3-3-3 compound 3C-3 (3B-3)

[M]+ = 482 3-3-4 compound 3C-4 (3B-4)

[M]+ = 524 3-3-5 compound 3C-5 (3B-5)

[M]+ = 558

Synthesis Example 3-3-No Synthesis of the Compound 3C-No

The compound 3B-No was dissolved in chloroform, and 1 equivalent ofN-bromo succinimide was added thereto, and agitated for 3 to 8 hours atnormal temperature. Distilled water was put into the reaction solution,the termination of the reaction was carried out, and the organic layerwas extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 3C-No.

3-3-1. Manufacturing of the Compound 3C-1

The compound 3B-1 (4.5 g, 12.18 mmol) was dissolved in chloroform (200mL), and N-bromo succinimide (2.17 g, 12.18 mmol) was added thereto, andagitated for 5 hours at normal temperature. Distilled water was put intothe reaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 3C-1 (4.7 g, yield86%).

3-3-2. Manufacturing of the Compound 3C-2

The compound 3B-2 (4.90 g, 12.12 mmol) was dissolved in chloroform (200mL), and N-bromo succinimide (2.17 g, 12.18 mmol) was added thereto, andagitated for 5 hours at normal temperature. Distilled water was put intothe reaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 3C-2 (5.5 g, yield86%).

Synthesis Example 3-3-No Manufacturing of the Compound 3C-No

In the manufacturing of the compound 3C-1 of Synthesis Example 3-2-1, itwas synthesized in the same method to manufacture the compound 3C-3,compound 3C-4, and compound 3C-5, except that the compound 3B-3,compound 3B-4, and compound 3B-5 were used instead of the compound 3B-1.

TABLE 14-1 Synthesis compound Example 3D-No 3-4-No (reactant) X —L1—Y0—L2—Y0 MS 3-4-1 compound 3D-1 (3C-1)

[M]+ = 479 3-4-2 compound 3D-2 (3C-2)

[M]+ = 555 3-4-3 compound 3D-3 (3C-3)

[M]+ = 513 3-4-4 compound 3D-4 (3C-4)

[M]+ = 555 3-4-5 compound 3D-5 (3C-5)

[M]+ = 589

Synthesis Example 3-4-No Synthesis of the Compound 3D-No

The compound 3C-1, and 1 to 1.5 equivalents of arylboronic acid (orboron ester) or the substituted or unsubstituted heteroarylboronic acid(or boron ester) were put, dissolved in THF, 0.02 equivalents ofPd(PPh₃) and 2 equivalents or more of 2M K₂CO₃/H₂O aqueous solution wereadded, and heated and agitated for 3 to 16 hours. The reaction mixturewas cooled to normal temperature, filtered or extracted with the organicsolvent, separated, purified, and dried to manufacture the 3D-Nocompound.

3-4-1. Manufacturing of the Compound 3D-1

After the compound 3C-1 (4.52 g, 10.48 mmol) and 4-chlorophenyl boronicacid (1.97 g, 12.57 mmol) were dissolved in THF (150 mL), Pd(PPh₃)₄(0.36 g, 0.31 mmol) and 70 ml of 2M K₂CO₃/H₂O aqueous solution were putthereinto and refluxed for 8 hours. Distilled water was put into thereaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 3D-1 (4.1 g, yield81%).

Synthesis Example 3-4-No Manufacturing of the Compound 3D-No

In Synthesis Example 3-4-1, it was synthesized in the same method tomanufacture the compound 3D-2, compound 3D-3, compound 3D-4, or compound3D-5, except that the compound 3C-2, compound 3C-3, compound 4C-1, orcompound 4C-2 were used instead of the compound 3C-1.

TABLE 15-1 Synthesis Example 4-1-No compound R6 yield(%) MS 4-1-1compound 4-A H 61 [M + H]+ = 220 4-1-2 compound 4-B H 96 [M + H]+ = 218

4-1-1. Manufacturing of the Compound 4-A

β-Tetralone (18 g, 123 mmol), and phenylhydrazine hydrochloride (11 g,76 mmol) were put into a small amount of acetic acid, and refluxed in150 mL of ethanol for 2 hours under nitrogen atmosphere. After they werecooled to normal temperature, the formed product was filtered and driedto manufacture the compound 4-A (16.5 g, yield 61%).

4-1-2. Manufacturing of the Compound 4-B

The compound 4-A (16.5 g, 75.34 mmol), and tetrachloro-1,4-benzoquinone(25.93 g, 105.5 mmol) were refluxed under the nitrogen atmosphere in 300ml of xylene for 2 hours. NaOH (10%) and water were put into thereaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 4-B (15.7 g, yield96%).

TABLE 16-1 Synthesis Example compound 4-1-No 4B-No —X MS 4-1-3 compound4B-1

[M + H]+ = 294 4-1-4 compound 4B-2

[M + H]+ = 370 4-1-5 compound 4B-3

[M + H]+ = 452

Synthesis Example 4-1-No Synthesis of the Compound 4B-No

The compound 4-1-No and 1 to 1.4 equivalents of substituted orunsubstituted aryl halide or substituted or unsubstituted heterohalidewere put, dissolved in xylene or toluene, and 1.4 to 2 equivalents ofsodium-tertiary-botoxide and 0.01 equivalents of Pd[P(t-Bu)₃]₂ wereadded thereto, and heated and agitated for 5 to 12 hours. The reactantswere cooled to normal temperature, filtered or extracted with theorganic solvent, separated, purified, and dried to manufacture the 4B-Nocompound.

4-1-3. Manufacturing of the Compound 4B-1

The compound 4B (10.1 g, 46.3 mmol), and bromobenzene (8.77 g, 55.6mmol) were dissolved in 200 ml of xylene, sodium-tertiary-botoxide (6.7g, 71.6 mmol), and Pd[P(t-Bu)₃]₂ (0.23 g, 0.463 mmol) were addedthereto, and refluxed for 7 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=7/1 solvent, it was agitated in petroleumether, and dried under vacuum to manufacture the compound 4B-1 (10.1 g,yield 74%).

4-1-4. Manufacturing of the Compound 4B-2

In the manufacturing of the compound 4B-1 of Synthesis Example 4-1-3, itwas synthesized in the same method to manufacture the compound 4B-2,except that the compound 4-bromoiodobiphenyl was used instead ofbromobenzene.

4-1-5. Manufacturing of the Compound 4B-3

In the manufacturing of the compound 4B-1 of Synthesis Example 4-1-3, itwas synthesized in the same method to manufacture the compound 4B-3,except that the compound S-14 was used instead of bromobenzene.

TABLE 17-1 Synthesis compound Example 4C-No 4-2-No (reactant) —X MS4-2-1 compound 4C-1 (4B-1)

[M]+ = 372 4-2-2 compound 4C-2 (4B-2)

[M]+ = 448 4-2-3 compound 4C-3 (4B-3)

[M]+ = 530

Synthesis Example 4-2-No Synthesis of the Compound 4C-No

The compound 2B-No was dissolved in chloroform, and 1 equivalent ofN-bromo succinimide was added thereto, and agitated for 3 to 5 hours atnormal temperature. Distilled water was put into the reaction solution,the termination of the reaction was carried out, and the organic layerwas extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 4C-No, and theresults are described in Table 14-1.

4-2-1. Manufacturing of the Compound 4C-1

The compound 4B-1 (9.5 g, 32.49 mmol) was dissolved in chloroform (300mL), and N-bromo succinimide (5.78 g, 32.49 mmol) was added thereto, andagitated for 5 hours at normal temperature. Distilled water was put intothe reaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 4C-1 (6.12 g, yield50%).

TABLE 18-1 Synthesis Example 4D-No MS 4-3-No (reactant) —X —L1—Y0 [M]+ =4-3-1 compound 4D-1 (4C-1)

403 4-3-2 compound 4D-2 (4C-1)

479 4-3-3 compound 4D-3 (4C-1)

485 4-3-4 compound 4D-4 (4C-2)

479 4-3-5 compound 4D-5 (4C-2)

555 4-3-6 compound 4D-6 (4C-3)

561

Synthesis Example 4-3-No Synthesis of the Compound 4D-No

The compound 4C-1, and 1 to 1.5 equivalents of the substituted orunsubstituted arylboronic acid (or boron ester) or substituted orunsubstituted heteroarylboronic acid (or boron ester) were put,dissolved in THF, 0.02 equivalents of Pd(PPh₃) and 2 equivalents or moreof 2M K₂CO₃/H₂O aqueous solution were added, and heated and agitated for3 to 16 hours. The reaction mixture was cooled to normal temperature,filtered or extracted with the organic solvent, separated, purified, anddried to manufacture the 4D-No compound, and the results thereof aredescribed in Table 18-1.

4-3-1. Manufacturing of the Compound 4D-1

After the compound 4C-1 (6.12 g, 16.45 mmol) and 4-chlorophenyl boronicacid (3.08 g, 19.74 mmol) were dissolved in THF (150 mL), Pd(PPh₃)₄(0.57 g, 0.49 mmol) and 70 ml of 2M K₂CO₃/H₂O aqueous solution were putthereinto and refluxed for 3 hours. Distilled water was put into thereaction solution, the termination was carried out, and the organiclayer was extracted. The reaction solution was concentrated, andrecrystallized with EtOH to manufacture the compound 4D-1 (4.1 g, yield62%).

4-3-2. Manufacturing of the Compound 4D-2

In the manufacturing of the compound 4D-1 of Synthesis Example 4-3-1, itwas synthesized in the same method to manufacture the compound 4D-2(6.73 g, yield 71%), except that 4-(4-chlorophenyl)phenyl boronic acid(4.59 g, 19.74 mmol) was used instead of 4-chlorophenyl boronic acid.

4-3-3. Manufacturing of the Compound 4D-3

In the manufacturing of the compound 4D-1 of Synthesis Example 4-3-1, itwas synthesized in the same method to manufacture the compound 4D-3(6.08 g, yield 76%), except that 5-(4-chlorophenyl)thiophenyl-2-boronicacid (4.32 g, 17.77 mmol) was used instead of 4-chlorophenyl boronicacid.

General Preparation Equation 1-No

General Preparation Example 1-No Manufacturing of the Compound 1-No

The compound 1C-No and 1.2 to 2.4 equivalents of substituted orunsubstituted arylamine or substituted or unsubstituted heteroarylamine,or substituted or unsubstituted aralkylamine were put, dissolved inxylene or toluene, and 1.0 to 4.0 equivalents ofsodium-tertiary-botoxide and 0.01 to 0.04 equivalents of Pd[P(t-Bu)₃]₂were added thereto, and heated and agitated for 5 to 12 hours. Thereactants were cooled to normal temperature, filtered or extracted withthe organic solvent, separated, purified, and dried to manufacture the1-No compound.

Preparation Example 1-1-No Manufacturing of the Compound Represented byFormula 1-1-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-1 was used as the compound 1C-No, the compound 1-1-No wasmanufactured by using the compound S-6, the arylamine compound S-1,S-34, S-16, S-24, S-30, S-26, and S-33, and the results are described inTable 1-1-1.

Preparation Example 1-1-1 Manufacturing of the Compound Represented byFormula 1-1-1

The compound 1-C-1 (3.57 g, 8.84 mmol), and compound S-6 (3.13 g, 9.72mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=10/1 solvent, it was agitated inpetroleum ether, and dried under vacuum to manufacture the compound 3that was represented by Formula 1-1-1 (3.4 g, yield 56%).

Preparation Example 1-1-2 Manufacturing of the Compound Represented byFormula 1-1-3

The compound 1-C-1 (3.57 g, 8.84 mmol), and compound S-1 (2.13 g, 9.72mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=10/1 solvent, it was agitated inpetroleum ether, and dried under vacuum to manufacture the compound thatwas represented by Formula 1-1-3 (2.6 g, yield 50%).

TABLE 1-1-1 Preparation Example product amine MS 1-1-No 1-1-No Reactant(Y1 − H) [M + H]+ = 1-1-1 1-1-1 1C-1 S-6  689 1-1-2 1-1-3 1C-1 S-1  5871-1-3 1-1-27 1C-1 S-3  565 1-1-4 1-1-21 1C-1 S-16 729 1-1-5 1-1-5 1C-1S-24 641 1-1-6 1-1-19 1C-1 S-30 653 1-1-7 1-1-9 1C-1 S-26 690 1-1-81-1-25 1C-1 S-33 780

Preparation Example 1-2-No Manufacturing of the Compound Represented byFormula 1-2-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-2 was used as the compound 1C-No, the compound 1-2-No wasmanufactured by using the compound S-6, the arylamine compound S-1, andS-30, and the results are described in Table 1-2-1.

Preparation Example 1-2-1 Manufacturing of the Compound Represented byFormula 1-2-1

The compound 1-C-2 (4.8 g, 10.0 mmol), and compound S-6 (3.54 g, 11.0mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=10/1 solvent, it was agitated inpetroleum ether, and dried under vacuum to manufacture the compound thatwas represented by Formula 1-2-1 (6.3 g, yield 82%).

TABLE 1-2-1 Preparation Example product amine MS 1-2-No 1-2-No reactant(Y1 − H) [M + H]+ = 1-2-1 1-2-1 1C-2 S-6  765 1-2-2 1-2-3 1C-2 S-1  6631-2-3 1-2-19 1C-2 S-30 729

Preparation Example 1-3-No Manufacturing of the Compound Represented byFormula 1-3-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-3 was used as the compound 1C-No, the compound 1-3-No wasmanufactured by using the compound S-6, the arylamine compound S-5,S-17, and S-35, the results are described in Table 1-3-1, and specificSynthesis Example 1-3-1 is shown.

Preparation Example 1-3-1 Manufacturing of the Compound Represented byFormula 1-3-1

The compound 1C-3 (4.3 g, 8.84 mmol), and compound S-6 (3.13 g, 9.72mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=10/1 solvent, it was agitated inpetroleum ether, and dried under vacuum to manufacture the compound thatwas represented by Formula 1-3-1 (4.2 g, yield 62%).

TABLE 1-3-1 Preparation Example product amine MS 1-3-No 1-3-No reactant(Y1 − H) [M + H]+ = 1-3-1 1-3-1 1C-3 S-6  771 1-3-2 1-3-85 1C-3 S-5  6191-3-3 1-3-84 1C-3 S-17 617 1-3-4 1-3-86 1C-3 S-35 784

Preparation Example 1-4-No Manufacturing of the Compound Represented byFormula 4-1-No Preparation Example 1-4-1 Manufacturing of the CompoundRepresented by Formula 4-1-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-4 was used as the compound 1C-No, the compound 4-1-No wasmanufactured by using the compound S-6, the arylamine compound S-17, andS-7, the results are described in Table 1-4-1, and specific SynthesisExample 4-1-1 is shown.

TABLE 1-4-1 Preparation Example product amine MS 4-1-No 1-4-No reactant(Y1 − H) [M + H]+ = 1-4-1 4-1-1 1C-4 S-6  881 1-4-2 4-1-84 1C-4 S-17 7271-4-3 4-1-88 1C-4 S-7  805

Preparation Example 1-5-No Manufacturing of the Compound Represented byFormula 3-1-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-5 was used as the compound 1C-No, the compound 3-1-No wasmanufactured by using the compound S-6, the arylamine compound S-1,S-40, S-16, S-24, and S-30, and the results are described in Table1-5-1.

Preparation Example 1-5-1 Manufacturing of the Compound Represented byFormula 3-1-1

The compound 1-C-5 (5.30 g, 11.05 mmol), and compound S-6 (3.91 g, 11.56mmol) were dissolved in 160 ml of xylene, sodium-tertiary-botoxide (1.59g, 16.58 mmol), and Pd[P(t-Bu)₃]₂ (0.056 g, 0.11 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 3-1-1 (7.6 g, yield 90%).

Preparation Example 1-5-2 Manufacturing of the Compound Represented byFormula 3-1-3

The compound 1C-1 (4.45 g, 8.66 mmol), and compound S-1 (2.09 g, 9.52mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.24g, 12.99 mmol), and Pd[P(t-Bu)₃]₂ (0.044 g, 0.086 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out with normal-hexane/ethylacetate=6/1 solvent, it was agitated in petroleum ether, and dried undervacuum to manufacture the compound that was represented by Formula 3-1-3(2.9 g, yield 50%).

TABLE 1-5-1 Preparation Example product amine MS 1-5-No 3-1-No reactant(Y1 − H) [M + H]+ = 1-5-1 3-1-1 1C-5 S-6  765 1-5-2 3-1-3 1C-5 S-1  6631-5-3 3-1-87 1C-5 S-40 703 1-5-4 3-1-21 1C-5 S-16 805 1-5-5 3-1-15 1C-5S-24 690 1-5-6 3-1-19 1C-5 S-30 729

Preparation Example 1-6-No Manufacturing of the Compound Represented byFormula 3-2-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-6 was used as the compound 1C-No, the compound 3-2-No wasmanufactured by using the arylamine compound such as the compound S-6,and the results are described in Table 1-6-1.

Preparation Example 1-6-1 Manufacturing of the Compound Represented byFormula 3-2-1

The compound 1-C-6 (5.07 g, 9.14 mmol), and compound S-6 (3.19 g, 10.0mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.31g, 13.66 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 3-2-1 (5.2 g, yield 67%).

TABLE 1-6-1 Preparation Example product amine MS 1-6-No 3-2-No reactant(Y1 − H) [M + H]+ = 1-6-1 3-2-1 1C-6 S-6 841 1-6-2  3-2-21 1C-6  S-16881

Preparation Example 1-7-No Manufacturing of the Compound Represented byFormula 3-3-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-7 was used as the compound 1C-No, the compound 3-3-No wasmanufactured by using the compound S-6, the arylamine compound S-5, andS-19, the results are described in Table 1-7-1, and specific PreparationExample 3-3-85 is shown.

Preparation Example 1-7-2 Manufacturing of the Compound Represented byFormula 3-3-85

The compound 1C-7 (4.97 g, 8.84 mmol), and compound S-5 (1.64 g, 9.72mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 3-3-85 (2.8 g, yield 46%).

TABLE 1-7-1 Preparation Example product amine MS 1-7-No 3-3-No reactant(Y1 − H) [M + H]+ = 1-7-1 3-3-1  1C-7 S-6 847 1-7-2 3-3-85 1C-7 S-5 6951-7-3 3-3-89 1C-7  S-19 770

Preparation Example 1-8-No Manufacturing of the Compound Represented byFormula 5-1-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-8 was used as the compound 1C-No, the compound 5-1-No wasmanufactured by using the compound S-6, substituted or unsubstitutedarylamine compound S-30, and S-1, the results are described in Table1-8-1, and specific Preparation Example 5-1-3 is shown.

Preparation Example 1-8-3 Manufacturing of the Compound Represented byFormula 5-1-3

The compound 1C-8 (4.97 g, 8.84 mmol), and compound S-1 (2.13 g, 9.72mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 5-1-3 (3.6 g, yield 55%).

TABLE 1-8-1 Preparation Example product amine MS 1-8-No 5-1-No reactant(Y1 − H) [M + H]+ = 1-8-1 5-1-1 1C-8 S-6 847 1-8-2  5-1-21 1C-8  S-16887 1-8-3 5-1-3 1C-8 S-1 745

Preparation Example 1-9-No Manufacturing of the Compound Represented byFormula 7-1-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-9 was used as the compound 1C-No, the compound 7-1-No wasmanufactured by using the compound S-3, the amine compound S-30, andS-1, the results are described in Table 1-9-1, and specific PreparationExample 1-9-1 is shown.

Preparation Example 1-9-1 Manufacturing of the Compound Represented byFormula 7-1-27

The compound 1C-9 (0.98 g, 7.07 mmol), and compound S-3 (1.54 g, 7.78mmol) were dissolved in 70 ml of xylene, sodium-tertiary-botoxide (1.02g, 10.6 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 7-1-27 (3.0 g, yield 59%).

TABLE 1-9-1 Preparation Example product amine MS 1-9-No 7-1-No reactant(Y1 − H) [M + H]+ = 1-9-1 7-1-27 1C-9 S-3 723 1-9-2 7-1-19 1C-9  S-30887 1-9-3 7-1-3  1C-9 S-1 745

Preparation Example 1-10-No Manufacturing of the Compound Represented byFormula 9-1-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-10 was used as the compound 1C-No, the compound 9-1-No wasmanufactured by using the compound S-6, the amine compound S-1, and S-6,the results are described in Table 1-10-1, and specific PreparationExample 1-10-2 is shown.

Preparation Example 1-10-2 Manufacturing of the Compound Represented byFormula 9-1-3

The compound 1C-10 (4.97 g, 10.61 mmol), and compound S-1 (3.2 g, 14.58mmol) were dissolved in 140 ml of xylene, sodium-tertiary-botoxide (1.91g, 19.89 mmol), and Pd[P(t-Bu)₃]₂ (0.068 g, 0.132 mmol) were addedthereto, and refluxed for 7 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 9-1-3 (3.8 g, yield 61%).

TABLE 1-10-1 Preparation Example product amine MS 1-10-No 9-1-Noreactant (Y1 − H) [M + H]+ = 1-10-1 9-1-1 1C-10 S-6 694 1-10-2 9-1-31C-10 S-1 592 1-10-3  9-1-21 1C-10  S-16 734

Preparation Example 1-11-No Manufacturing of the Compound Represented byFormula 14-1-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-11 was used as the compound 1C-No, the compound 14-1-No wasmanufactured by using the compound S-6, the amine compound S-1, andS-16, the results are described in Table 1-11-1, and specificPreparation Example 1-11-1 is shown.

Preparation Example 1-11-1 Manufacturing of the Compound Represented byFormula 14-1-1

The compound 1C-11 (3.80 g, 9.0 mmol), and compound S-6 (3.13 g, 9.72mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 14-1-1 (4.64 g, yield 73%).

TABLE 1-11-1 Preparation Example product amine MS 1-11-No 14-1-Noreactant (Y1 − H) [M + H]+ = 1-11-1 14-1-1  1C-11 S-6 707 1-11-2 14-1-3 1C-11 S-1 605 1-11-3 14-1-21 1C-11  S-16 747

Preparation Example 1-12-No Manufacturing of the Compound Represented byFormula 11-1-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-12 was used as the compound 1C-No, the compound 11-1-No wasmanufactured by using the compound S-6, substituted or unsubstitutedarylamine compound S-19, and S-35, the results are described in Table1-12-1, and specific Preparation Example 1-12-1 is shown.

Preparation Example 1-12-1 Manufacturing of the Compound Represented byFormula 11-1-1

The compound 1C-12 (4.86 g, 8.70 mmol), and compound S-6 (3.13 g, 9.72mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 11-1-1 (4.64 g, yield 73%).

TABLE 1-12-1 Preparation Example product amine MS 1-12-No 11-1-Noreactant (Y1 − H) [M + H]+ = 1-12-1 11-1-1  1C-12 S-6  844 1-12-211-1-89 1C-12 S-19 767 1-12-3 11-1-86 1C-12 S-35 857

Preparation Example 1-13-No Manufacturing of the Compound Represented byFormula 12-1-No

In the general method of the compound 1-No of Preparation Example 1-No,1C-13 was used as the compound 1C-No, the compound 12-1-No wasmanufactured by using the compound S-6, the amine compound S-5, andS-27, the results are described in Table 1-13-1, and specificPreparation Example 1-13-1 is shown.

Preparation Example 1-13-1 Manufacturing of the Compound Represented byFormula 12-1-85

The compound 1C-13 (5.72 g, 9.0 mmol), and compound S-5 (1.69 g, 10.0mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 12-1-85 (4.7 g, yield 68%).

TABLE 1-13-1 Preparation Example product amine MS 1-13-No 12-1-Noreactant (Y1 − H) [M + H]+ = 1-13-1 12-1-85 1C-13 S-5  768 1-13-212-1-84 1C-13 S-17 766

General Preparation Equation 2-No

General Preparation Example 2-No Manufacturing of the CompoundRepresented by Formula 2-No

In the general method of the compound 1-No of Preparation Example 1-No,2D-No was used as the compound 1C-No, the compound 2-No was manufacturedby using the compound S-6, the substituted or unsubstituted arylaminecompound, the results are described in Table 2-1-1, Table 2-2-1, Table2-3-1, Table 2-5-1, Table 2-6-1, Table 2-7-1, Table 2-8-1, Table 2-9-1,Table 2-10-1, and Table 2-11-1, and specific Preparation Examples 2-1-1and Preparation Example 2-5-1, and Preparation Example 2-5-4 are shown.

Preparation Example 2-1-1 Manufacturing of the Compound Represented byFormula 1-21-1

The compound 2D-1 (4.04 g, 10.0 mmol), and compound S-6 (3.85 g, 12.0mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (1.44g, 14.98 mmol), and Pd[P(t-Bu)₃]₂ (0.050 g, 0.099 mmol) were addedthereto, and refluxed for 7 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 1-21-1 (4.96 g, yield 72%).

TABLE 2-1-1 Preparation Example product amine MS 2-1-No 1-21-No reactant(Y1 − H) [M + H]+ = 2-1-1 1-21-1 2D-1 S-6  689 2-1-2 1-21-3 2D-1 S-1 587 2-1-3  1-27-27 2D-1 S-3  565 2-1-4  1-21-21 2D-1 S-16 729 2-1-51-21-5 2D-1 S-24 641 2-1-6  1-21-19 2D-1 S-30 653 2-1-7 1-21-9 2D-1 S-26690

TABLE 2-2-1 Preparation Example product amine MS 2-2-No 1-22-No reactant(Y1 − H) [M + H]+ = 2-2-1 1-22-1  2D-2 S-6 765 2-2-2 1-22-3  2D-2 S-1663 2-2-3 1-22-19 2D-2  S-30 729

TABLE 2-3-1 Preparation Example product amine MS 2-3-No 1-23-No reactant(Y1 − H) [M + H]+ = 2-3-1 1-23-1  2D-3 S-6  771 2-3-2 1-23-27 2D-3 S-5 619 2-3-3 1-23-28 2D-3 S-17 617 2-3-4 1-23-29 2D-3 S-35 784

Preparation Example 2-5-1 Manufacturing of the Compound Represented byFormula 3-21-1

The compound 2D-5 (4.80 g, 10.0 mmol), and compound S-6 (4.02 g, 12.5mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (1.44g, 14.98 mmol), and Pd[P(t-Bu)₃]₂ (0.050 g, 0.099 mmol) were addedthereto, and refluxed for 7 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 3-21-1 (5.05 g, yield 66%).

Preparation Example 2-5-4 Manufacturing of the Compound Represented byFormula 3-21-21

The compound 2D-5 (4.80 g, 10.0 mmol), and compound S-16 (4.34 g, 12.0mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (1.44g, 14.98 mmol), and Pd[P(t-Bu)₃]₂ (0.050 g, 0.099 mmol) were addedthereto, and refluxed for 7 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 3-21-21 (4.30 g, yield 59%).

TABLE 2-5-1 Preparation Example product amine MS 2-5-No 3-21-No reactant(Y1 − H) [M + H]+ = 2-5-1 3-21-1  2D-5 S-6  765 2-5-2 3-21-3  2D-5 S-1 663 2-5-3 3-21-5  2D-5 S-3  703 2-5-4 3-21-21 2D-5 S-16 805 2-5-53-21-15 2D-5 S-24 690 2-5-6 3-21-19 2D-5 S-30 729

TABLE 2-6-1 Preparation Example product amine MS 2-6-No 3-22-No reactant(Y1 − H) [M + H]+ = 2-6-1 3-22-1  2D-6 S-6 841 2-6-2 3-22-21 2D-6 S-30889

TABLE 2-7-1 Preparation Example product amine MS 2-7-No 3-23-No reactant(Y1 − H) [M + H]+ = 2-7-1 3-23-1  2D-7 S-6 847 2-7-2 3-23-27 2D-7 S-5695 2-7-3 3-23-28 2D-7  S-19 770

TABLE 2-8-1 Preparation Example product amine MS 2-8-No 5-21-No reactant(Y1 − H) [M + H]+ = 2-8-1 5-21-1 2D-8 S-6 848 2-8-2  5-21-21 2D-8  S-16887 2-8-3 5-21-3 2D-8 S-1 745

TABLE 2-9-1 Preparation Example product amine MS 2-9-No 9-21-No reactant(Y1 − H) [M + H]+ = 2-9-1 9-21-27 2D-9 S-3  723 2-9-2 9-21-21 2D-9 S-30887 2-9-3 9-21-3  2D-9 S-1  745

TABLE 2-10-1 Preparation Example product amine MS 2-10-No 14-21-Noreactant (Y1 − H) [M + H]+ = 2-10-1 14-21-1  2D-10 S-6  694 2-10-214-21-3  2D-10 S-1  592 2-10-3 14-21-21 2D-10 S-16 734

TABLE 2-11-1 Preparation Example product amine MS 2-11-No 12-21-Noreactant (Y1 − H) [M + H]+ = 2-11-1 12-21-1  2D-11 S-6  707 2-11-212-21-3  2D-11 S-1  605 2-11-3 12-21-21 2D-11 S-16 747

Preparation Equation 3-No

Preparation Example 3-No Manufacturing of the Compound Represented byFormula 3-No

In the general method of the compound 1-No of Preparation Example 1-No,2F-No or 3D-No was used instead of the compound 1C-No, the compound [1or 3]-No was manufactured by using the compound S-6, and the aminecompound, the results are described in Table 3-1-1, and specificPreparation Examples 3-1-1 and 3-1-3 are shown.

Preparation Example 3-1-1 Manufacturing of the Compound Represented byFormula 1-201-1

The compound 2-F-1 (4.1 g, 9.0 mmol), and compound S-6 (3.47 g, 10.8mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (1.30g, 13.48 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.081 mmol) were addedthereto, and refluxed for 7 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 1-201-1 (4.61 g, yield 67%).

Preparation Example 3-1-3 Manufacturing of the Compound Represented byFormula 1-301-1

The compound 2F-3 (4.8 g, 10.0 mmol), and compound S-6 (3.85 g, 12.0mmol) were dissolved in 100 ml of xylene, sodium-tertiary-botoxide (1.44g, 14.98 mmol), and Pd[P(t-Bu)₃]₂ (0.050 g, 0.099 mmol) were addedthereto, and refluxed for 12 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 1-301-1 (4.28 g, yield 56%).

TABLE 3-1-1 Preparation Example product amine MS 3-1-No [1 or 3]-Noreactant (Y1 − H) [M + H]+ = 3-1-1 1-201-1 2F-1 S-6 765 3-1-2 1-101-12F-3 S-6 765 3-1-3 1-301-1 3D-1 S-6 765 3-1-4 3-301-1 3D-4 S-6 841 3-1-53-101-1 2F-10 S-6 841

Preparation Equation 1-4

Preparation Example 4-No Manufacturing of the Compound Represented byFormula 4-No

In the general method of the compound 1-No of Preparation Example 1-No,4D-No was used as the compound 1C-No, the compound 4-No was manufacturedby using the compound S-6, substituted or unsubstituted arylaminecompound, the results are described in Table 4-1-1, Table 4-2-1, Table4-3-1, Table 4-4-1, and Table 4-5-1, and specific Preparation Example4-1-1 is shown.

Preparation Example 4-1-1 Manufacturing of the Compound Represented byFormula 4-1-1

The compound 4D-1 (5.25 g, 13.0 mmol), and compound S-6 (5.01 g, 15.6mmol) were dissolved in 120 ml of xylene, sodium-tertiary-botoxide (1.87g, 19.47 mmol), and Pd[P(t-Bu)₃]₂ (0.065 g, 0.13 mmol) were addedthereto, and refluxed for 7 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 4-1-1 (6.09 g, yield 68%).

TABLE 4-1-1 Preparation Example product amine MS 4-1-No 1-41-No reactant(Y1 − H) [M + H]+ = 4-1-1 1-41-1  4D-1 S-6  689 4-1-2 1-41-3  4D-1 S-1 587 4-1-3 1-41-27 4D-1 S-3  565 4-1-4 1-41-21 4D-1 S-16 729

TABLE 4-2-1 Preparation Example product amine MS 4-2-No 1-42-No reactant(Y1 − H) [M + H]+ = 4-2-1 1-42-1  4D-2 S-6  765 4-2-2 1-42-3  4D-2 S-1 663 4-2-3 1-42-19 4D-2 S-30 729

TABLE 4-3-1 Preparation Example product amine MS 4-3-No 1-43-No reactant(Y1 − H) [M + H]+ = 4-3-1 1-43-1  4D-3 S-6  771 4-3-2 1-43-86 4D-3 S-35784

TABLE 4-4-1 Preparation Example product amine MS 4-4-No 3-41-No reactant(Y1 − H) [M + H]+ = 4-4-1 3-41-1  4D-4 S-6  881 4-4-2 3-41-84 4D-4 S-17727

TABLE 4-5-1 Preparation Example product amine MS 4-5-No 3-42-No reactant(Y1 − H) [M + H]+ = 4-5-1 3-42-1  4D-5 S-6  765 4-5-2 3-42-3  4D-5 S-1 663 4-5-3 3-42-5  4D-5 S-3  703 4-5-4 3-42-21 4D-5 S-16 805

General Preparation Equation 1-5

Preparation Example 5-No Manufacturing of the Compound Represented byFormula 5-No

In the general method of the compound 1-No of Preparation Example 1-No,5B-No was used as the compound 1C-No, the compound 5-No was manufacturedby using the compound S-6, substituted or unsubstituted arylaminecompound, the results are described in Table 5-1-1, and Table 5-5-1, andspecific Preparation Example 5-1-1 is shown.

Preparation Example 5-1-1 Manufacturing of the Compound Represented byFormula 1-61-1

The compound 3B-2 (3.57 g, 8.84 mmol), and compound S-6 (3.22 g, 10.00mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=8/1 solvent, it was agitated in petroleumether, and dried under vacuum to manufacture the compound that wasrepresented by Formula 1-61-1 (3.28 g, yield 54%).

TABLE 5-1-1 Preparation Example product amine MS 5-1-No 1-61-No reactant(Y1 − H) [M + H]+ = 5-1-1 1-61-1  3B-2 S-6  689 5-1-2 1-61-3  3B-2 S-1 587 5-1-3 1-61-27 3B-2 S-3  565 5-1-4 1-61-21 3B-2 S-16 729

Preparation Example 5-5-1 Manufacturing of the Compound Represented byFormula 3-61-1

The compound 3B-5 (4.16 g, 8.66 mmol), and compound S-6 (2.93 g, 9.12mmol) were dissolved in 150 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Itwas dissolved in ethyl acetate, crystallized with ethanol, filtered, anddried under vacuum to manufacture the compound that was represented byFormula 3-61-1 (6.45 g, yield 72%).

TABLE 5-5-1 Preparation Example product amine MS 5-5-No 3-61-No reactant(Y1 − H) [M + H]+ = 5-5-1 3-61-1  3B-5 S-6  765 5-5-2 3-61-3  3B-5 S-1 663 5-5-3 3-61-5  3B-5 S-3  703 5-5-4 3-61-21 3B-5 S-16 805

General Preparation Equation 1-6

General Preparation Example 6-No Manufacturing of the CompoundsRepresented by Formula A-11-No, A-32-No, and A-51-No

The compounds A-11-No, A-32-No, and A-51-No was manufactured by usingabout 0.45 equivalents of compound 1-B-No, 2C-No, or 4C-No andsubstituted or unsubstituted arylamine, heteroarylamine, oraralkyldiamine, or 1.2 to 2.0 equivalents of the compound 1-B-No, 2C-No,or 4C-No and arylamine, heteroarylamine, and aralkylamine that weresubstituted by the arylamino group, and the results are described inTable 6-1-1.

Preparation Example 6-1-1 Manufacturing of the Compound Represented byFormula 1-11-36

The compound 1-B-1 (3.72 g, 10.0 mmol), and compound S-37 (1.51 g, 4.5mmol) were dissolved in 50 ml of xylene, sodium-tertiary-botoxide (1.27g, 13.26 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=4/1 solvent, it was agitated in petroleumether, and dried under vacuum to manufacture the compound that wasrepresented by Formula 1-11-36 (3.31 g, yield 36%).

Preparation Example 6-1-1 Manufacturing of the Compound Represented byFormula 1-11-42

The compound 1-B-1 (3.72 g, 10.0 mmol), and compound S-38 (6.12 g, 10.6mmol) were dissolved in 50 ml of xylene, sodium-tertiary-botoxide (1.44g, 15.0 mmol), and Pd[P(t-Bu)₃]₂ (0.045 g, 0.088 mmol) were addedthereto, and refluxed for 5 hours under the nitrogen atmosphere.Distilled water was put into the reaction solution, the termination ofthe reaction was carried out, and the organic layer was extracted. Afterthe column separation was carried out withnormal-hexane/tetrahydrofurane=4/1 solvent, it was agitated in petroleumether, and dried under vacuum to manufacture the compound that wasrepresented by Formula 1-11-42 (5.1 g, yield 59%).

TABLE 6-1-1 Preparation Example amine MS 6-1-No product reactant (Y1 −H) [M + H]+ = 6-1-1 1-11-36 1-B-1 S-37 919 6-1-2 1-11-42 1-B-1 S-38 8696-1-3 1-32-44 2C-1 S-37 919 6-1-4 1-32-40 2C-1 S-39 779 6-1-5 1-32-422C-1 S-38 869 6-1-6 1-51-37 4C-1 S-37 919

Example 1-1

A glass substrate (corning 7059 glass) on which a thin film of ITO(indium tin oxide) was coated to a thickness of 1,000 Å was immersed indistilled water having a detergent dissolved therein to wash thesubstrate with ultrasonic waves. The detergent as used herein was aproduct commercially available from Fisher Co. and the distilled waterwas one which had been twice filtered by using a filter commerciallyavailable from Millipore Co. ITO was washed for 30 minutes, and thenwashing with ultrasonic waves was repeated twice for 10 minutes by usingdistilled water. After the completion of washing with distilled water,washing with ultrasonic waves was subsequently carried out by usingsolvents such as isopropyl alcohol, acetone and methanol, and theresultant product was dried.

On the ITO transparent electrode thus prepared, hexanitrilehexaazatriphenylene was coated to thicknesses of 500 Å by thermal vacuumdeposition to form a hole injecting layer. After the compound (400 Å)that was the material transporting the holes, synthesized in PreparationExample 1, and represented by Formula 1-1-1 was deposited under thevacuum thereon, the host H1 and the dopant compound D1 were depositedunder the vacuum as the light emitting layer in a thickness of 300 Å.Thereafter, the E1 compound (300 Å) was deposited by heating under thevacuum as the electron injection and the transport layer. On theelectron transport layer, lithium fluoride (LiF) in a thickness of 12 Åand aluminium in a thickness of 2,000 Å were subsequently deposited toform a cathode, thereby manufacturing the organic light emitting device.

In the above process, the deposition speed of the organic material wasmaintained at 1 Å/sec, that of lithium fluoride was maintained at 0.2Å/sec, and that of aluminium was maintained at 3 to 7 Å/sec.

Example 1-2 to Example 1-28

The organic light emitting device was manufactured by using thecompounds that were manufactured in Preparation Examples and representedby Formula 1-1-3, Formula 1-1-19, Formula 1-1-21, Formula 4-1-1, Formula3-1-1, Formula 3-1-21, Formula 3-2-1, Formula 9-1-1, Formula 9-1-21,Formula 14-1-1, Formula 13-1-1, Formula 3-2-1, Formula 3-2-3, Formula3-2-21, Formula 3-22-1, Formula 3-22-21, Formula 9-21-3, Formula14-21-1, Formula 12-21-6, Formula 1-201-1, Formula 1-101-1, Formula1-301-1, Formula 1-41-1, Formula 1-42-1, Formula 3-41-84, Formula1-61-1, Formula 3-61-16, Formula 1-11-36, Formula 1-11-42, Formula1-32-44, Formula 1-32-42, Formula 1-32-40, and Formula 1-51-37 insteadof the compound that was represented by Formula 1-1-1 in Example 1-1,and using the compound E1.

Comparative Example 1

The same experiment was carried out, except that NPB was used instead ofthe compound that was synthesized as the hole transport layer inPreparation Example and represented by Formula 1-1-1 in Example 1-1.

Comparative Example 2

The same experiment was carried out, except that HT1 was used instead ofthe compound that was synthesized as the hole transport layer inPreparation Example and represented by Formula 1-1-1 in Example 1-1.

The test results of the organic light emitting devices that weremanufactured by using each compound as the hole transport layer materiallike Example 1-1 are described in the following Table 1.

TABLE 1 Experimental Current Color Example voltage efficiency coordinate100 mA/cm² HTL (V) (cd/A) (x, y) Comparative NPB 8.38 26.59 (0.314,0.650) Example 1 Comparative HT1 9.12 23.89 (0.312, 0.651) Example 2Example 1-1 Formula 1-1-1 7.57 24.57 (0.311, 0.650) Example 1-2 Formula1-1-3 6.76 26.44 (0.312, 0.650) Example 1-3 Formula 1-1-19 8.22 28.59(0.317, 0.651) Example 1-4 Formula 1-1-21 6.91 25.27 (0.310, 0.652)Example 1-5 Formula 4-1-1 8.29 28.63 (0.318, 0.653) Example 1-6 Formula3-1-1 8.28 28.61 (0.318, 0.652) Example 1-7 Formula 3-1-21 7.31 29.12(0.318, 0.658) Example 1-8 Formula 3-2-1 7.12 27.34 (0.319, 0.657)Example 1-9 Formula 9-1-1 8.19 27.65 (0.318, 0.658) Example 1-10 Formula9-1-21 8.37 29.52 (0.318, 0.653) Example 1-11 Formula 14-1-1 8.31 28.91(0.317, 0.651) Example 1-12 Formula 13-1-1 8.32 28.98 (0.317, 0.653)Example 1-13 Formula 3-2-1- 7.29 27.35 (0.314, 0.651) Example 1-14Formula 3-2-3 7.57 24.57 (0.311, 0.650) Example 1-15 Formula 3-2-21 7.4128.78 (0.318, 0.653) Example 1-16 Formula 3-22-1 8.42 28.81 (0.319,0.654) Example 1-17 Formula 3-22-21 8.29 28.63 (0.318, 0.653) Example1-18 Formula 9-21-3 7.71 24.58 (0.311, 0.650) Example 1-19 Formula14-21-1 8.21 28.63 (0.317, 0.652) Example 1-20 Formula 12-21-6 6.7126.38 (0.311, 0.652) Example 1-21 Formula 1-201-1 6.76 27.31 (0.312,0.651) Example 1-22 Formula 1-101-1 8.30 27.39 (0.315, 0.651) Example1-23 Formula 1-301-1 6.78 26.40 (0.314, 0.651) Example 1-24 Formula1-41-1 6.81 26.21 (0.312, 0.651) Example 1-25 Formula 1-42-1 6.68 23.40(0.313, 0.650) Example 1-26 Formula 3-41-84 6.81 26.08 (0.312, 0.651)Example 1-27 Formula 1-61-1 7.03 26.49 (0.314, 0.649) Example 1-28Formula 3-61-1 7.12 28.01 (0.314, 0.651) Example 1-29 Formula 1-11-368.08 27.63 (0.318, 0.653) Example 1-30 Formula 1-11-42 7.97 28.53(0.317, 0.650) Example 1-31 Formula 1-32-44 7.78 26.62 (0.317, 0.652)Example 1-32 Formula 1-32-40 7.54 25.43 (0.316, 0.652) Example 1-33Formula 1-32-42 8.12 27.01 (0.312, 0.651) Example 1-34 Formula 1-51-377.09 28.63 (0.318, 0.649) Example 1-35 Formula 3-101-1 8.59 26.58(0.315, 0.652)

The compound that is represented by Formula 1 according to the presentinvention can function to inject and transport holes in the organiclight emitting device and the organic electronic device, and the deviceaccording to the present invention shows excellent characteristics inviews of efficiency, the driving voltage, and stability.

Example 2-1

A glass substrate (corning 7059 glass) on which a thin film of ITO(indium tin oxide) was coated to a thickness of 1,000 Å was immersed indistilled water having a detergent dissolved therein to wash thesubstrate with ultrasonic waves. The detergent as used herein was aproduct commercially available from Fisher Co. and the distilled waterwas one which had been twice filtered by using a filter commerciallyavailable from Millipore Co. ITO was washed for 30 minutes, and thenwashing with ultrasonic waves was repeated twice for 10 minutes by usingdistilled water. After the completion of washing with distilled water,washing with ultrasonic waves was subsequently carried out by usingsolvents such as isopropyl alcohol, acetone and methanol, and theresultant product was dried.

On the ITO transparent electrode thus prepared, hexanitrilehexaazatriphenylene was coated to thicknesses of 200 Å by thermal vacuumdeposition to form a hole injecting layer. After the compound (300 Å)that was the material injecting the holes, synthesized in PreparationExample 10, and represented by Formula 1-1-25 was deposited under thevacuum thereon, NPB (400 Å) was deposited under the vacuum as the holetransport layer. The host H1 and the dopant compound D1 were depositedunder the vacuum as the light emitting layer in a thickness of 300 Å.Thereafter, the E1 compound (300 Å) was subsequently deposited byheating under the vacuum as the electron injection and the transportlayer. On the electron transport layer, lithium fluoride (LiF) in athickness of 12 Å and aluminium in a thickness of 2,000 Å weresubsequently deposited to form a cathode, thereby manufacturing theorganic light emitting device.

In the above process, the deposition speed of the organic material wasmaintained at 1 Å/sec, that of lithium fluoride was maintained at 0.2Å/sec, and that of aluminium was maintained at 3 to 7 Å/sec.

Example 2-1 to 2-6

The organic light emitting device was manufactured by using thecompounds that were manufactured in Preparation Examples and representedby Formula 5-1-1, Formula 5-1-21, Formula 5-21-21, Formula and 5-21-3,and Formula 1-51-37 instead of the compound that was represented byFormula 1-1-25 in Example 2-1, and using the compound E1, and the testresults are described in the following Table 2.

TABLE 2 Experimental Current Example HA(200 Å)/ voltage efficiency Colorcoordinate 100 mA/cm² HIL(300 Å) (V) (cd/A) (x, y) Comparative HA 8.3826.59 (0.314, 0.650) Example 1 Example 2-1 Formula 1-1-25 8.11 28.63(0.317, 0.652) Example 2-2 Formula 5-1-1 7.98 26.31 (0.318, 0.652)Example 2-3 Formula 5-1-21 8.22 28.59 (0.317, 0.651) Example 2-4 Formula5-21-21 8.06 28.63 (0.318, 0.653) Example 2-5 Formula 5-21-3 7.29 24.66(0.318, 0.657)

As shown in Examples, in the case of when the manufactured compounds areused as the hole transport layer (HTL), in Formula 1, it is preferablethat X that is the 9-position substituent of N-carbazole is not thesubstituted or unsubstituted arylaminoaryl group, but X that is the9-position substituent of N-carbazole was is the aryl group such as thephenyl group, and the biphenyl group, and it is preferable that R1 to R8are the substituted or unsubstituted arylamino group, or thearylaminoarylene group.

In Formula 1, the preferable compounds as the hole injection layer (HIL)are materials that have substituents having the HOMO values capable ofbeing smaller than that of the hole transport layer (HTL). That is, inorder to allow the carrier to easily move from the anode such as ITO(indium tin oxide) to the hole transport layer (HTL), it is preferablethat the length of conjugation is increased, or the materials comprisingthe arylamino group, the arylaminoaryl group, or the thiophenyl groupare substituted so as to change their properties into the p-typematerials. In particular, the compounds according to the presentinvention can be used as the hole injection layer, thus obtaining theexcellent result.

In Comparative Example 1 of Table 1, in the case of the compound of H1,the arylaminoallyl group is disposed at carbazole-N-9. On the otherhand, the compounds of examples of Table 1, Table 2 and Table 3 are thearylamino group and the arylaminoaryl group, of which R1 to R8 aresubstituted or unsubstituted, and the aryl group which is substituted bythiophenyl, and most of them are the compound in which X ofcarbazole-N-9 is the aryl group. From the results, it can be seen thatmore excellent performance results are obtained.

The reason for this is that when the electrons moving from the electrodethrough the electron injection and the electron transport layer (ETL) tothe light emitting layer (EML) reach the interface of the hole transportlayer (HTL), the aryl group is more stable than the arylamino group. Thearylamino group is stable in the hole but weak to the electron, suchthat it can negatively affect efficiency and a lifespan of the organicelectronic device.

On the other hand, in the compound H1, since the distribution ofelectrons is disposed at the arylamino group, phenyl group of theN-9-positions, stability may be low. It can be deemed that the electronsdistributed at the aryl group such as the phenyl group, naphthyl groupand the biphenyl group, not the electrons at the arylamino group canprovide stability to the organic electronic device. Accordingly, thecompounds that are represented by Formula 1 used as the hole transportlayer (HTL), and as the substituent at the carbazole-N-9-position, thearyl group or the heteroaryl group is preferable, and particularly, thearyl group is preferable. In the case of when the compounds that arerepresented by Formula 1 are used as the hole injection layer (HIL),since the hole transport layer (HTL) is disposed between the holeinjection layer (HIL) and the light emitting layer (EML), even thoughthe aryl group in which the arylamino group is introduced at thecarbazole-N-9-position is used as the hole injection layer (HIL), thehole transport layer (HTL) can stop the electrons, such that it cannotlargely affect the device even though the substitutents such as thearylamino group and the thiophenyl group are introduced. In particular,since the substitutents such as the arylamino group and the thiophenylgroup can produce the holes, they are preferable as the hole transportlayer (HIL).

Example 3-1

A glass substrate (corning 7059 glass) on which a thin film of ITO(indium tin oxide) was coated to a thickness of 1,000 Å was immersed indistilled water having a detergent dissolved therein to wash thesubstrate with ultrasonic waves. The detergent as used herein was aproduct commercially available from Fisher Co. and the distilled waterwas one which had been twice filtered by using a filter commerciallyavailable from Millipore Co. ITO was washed for 30 minutes, and thenwashing with ultrasonic waves was repeated twice for 10 minutes by usingdistilled water. After the completion of washing with distilled water,washing with ultrasonic waves was subsequently carried out by usingsolvents such as isopropyl alcohol, acetone and methanol, and theresultant product was dried.

On the ITO transparent electrode thus prepared, hexanitrilehexaazatriphenylene was coated to thicknesses of 500 Å by thermal vacuumdeposition to form a hole injecting layer. After the compound (400 Å)that was the material transporting the holes, synthesized in PreparationExample 2-1-1, and represented by Formula 1-21-1 was deposited under thevacuum thereon. The host H2 and the dopant compound D3 (dopingconcentration 14%) were deposited under the vacuum as the light emittinglayer in a thickness of 300 Å. Thereafter, the E1 compound (300 Å) wassubsequently deposited by heating under the vacuum as the electroninjection and the transport layer. On the electron transport layer,lithium fluoride (LiF) in a thickness of 12 Å and aluminium in athickness of 2,000 Å were subsequently deposited to form a cathode,thereby manufacturing the organic light emitting device.

In the above process, the deposition speed of the organic material wasmaintained at 1 Å/sec, that of lithium fluoride was maintained at 0.2Å/sec, and that of aluminium was maintained at 3 to 7 Å/sec.

Example 3-2 to 3-4

The organic light emitting device was manufactured by using thecompounds that were manufactured in Preparation Examples and representedby Formula 11-1-1, Formula 11-1-89, Formula 11-1-86, Formula 12-1-85,Formula 12-1-84, Formula 12-21-1, Formula 12-21-3, and Formula 12-21-21instead of the compound that was represented by Formula H3 in Example3-1, and using the compound E1, and the test results are described inthe following Table 3.

TABLE 3 Experimental Current Example EML voltage efficiency Colorcoordinate 20 mA/cm² (Host: D3) (V) (cd/A) (x, y) Comparative H3 6.41 6.08 (0.325, 0.618) Example 5 Example 5-1 Formula 11-1-1 4.89  9.48(0.412, 0.562) Example 5-2 Formula 11-1-89 5.52 22.57 (0.354, 0.611)Example 5-3 Formula 11-1-86 4.31 39.07 (0.362, 0.607) Example 5-4Formula 12-1-85 4.57 36.96 (0.380, 0.589) Example 5-5 Formula 12-1-845.74 38.08 (0.371, 0.595) Example 5-6 Formula 12-21-1 4.46 32.16 (0.365,0.601) Example 5-7 Formula 12-21-3 4.61 27.46 (0.360, 0.603) Example 5-8Formula 12-21-21 4.88 30.46 (0.365, 0.603)

As shown in Table 3, the compound derivative that is represented byFormula according to the present invention can function as the lightemitting material in the organic light emitting device and the organicelectronic device, and the device according to the present inventionshows excellent characteristics in views of efficiency, the drivingvoltage, and stability. In particular, in views of efficiency, the highlight emitting characteristics are shown.

The invention claimed is:
 1. A compound that is represented by thefollowing Formula 1:

wherein R¹ and R² are bonded to each other to form an aromatic ring orR³ and R⁴ are bonded to each other to form an aromatic ring, or R¹ andR² are bonded to each other to form an aromatic ring while R³ and R⁴ arebonded to each other to form an aromatic ring, at least one of thefollowing groups is -(L1)p-(Y1)q: (1) a substituent group which is notformed into an aromatic ring among R¹ to R⁴, (2) R⁵ to R⁸, (3) asubstituent group that is substituted at an aromatic ring that is formedby bonding R¹ and R² to each other, and (4) a substituent group that issubstituted at an aromatic ring that is formed by bonding R³ and R⁴ toeach other, p is an integer in the range of 0 to 10, and q is an integerin the range of 1 to 10, the remains are each independently-(L2)r-(Y2)s, r is an integer in the range of 0 to 10, and s is aninteger in the range of 1 to 10, X is a fluoranthene or-(A)_(m)-(B)_(n), m is an integer in the range of 1 to 10, and n isindependently an integer in the range of 1 to 10, A is a substituted orunsubstituted phenylene group; a substituted or unsubstitutedbiphenylene group; a substituted or unsubstituted naphthylene group; asubstituted or unsubstituted alkenylene group; a substituted orunsubstituted fluorenylene group; or a substituted or unsubstitutedheteroarylene group that comprises one or more of N, O and S atoms, B isdeuterium; halogen group; nitrile group; nitro group; hydroxy group;substituted or unsubstituted alkyl group; substituted or unsubstitutedcycloalkyl group; substituted or unsubstituted alkoxy group; substitutedor unsubstituted aryloxy group; substituted or unsubstituted alkylthioxygroup; substituted or unsubstituted arylthioxy group; substituted orunsubstituted alkylsulfoxy group; substituted or unsubstitutedarylsulfoxy group; substituted or unsubstituted alkenyl group;substituted or unsubstituted silyl group; substituted or unsubstitutedboron group; substituted or unsubstituted phenyl group; a substituted orunsubstituted biphenyl group; a substituted or unsubstituted naphthylgroup; substituted or unsubstituted fluorenyl group; or substituted orunsubstituted hetero ring group having one or more of N, O and S atoms,when R³ and R⁴ are bonded to each other to form an aromatic ring and R¹and R² are not bonded to each other to form an aromatic ring, in thecase of X is aryl group, the number of carbon atoms of X is 30 or less,L1 is substituted or unsubstituted arylene group; substituted orunsubstituted alkenylene group; substituted or unsubstitutedfluorenylene group; substituted or unsubstituted carbazolylene group; orsubstituted or unsubstituted heteroarylene group having one or more ofN, O and S atoms, L2 is substituted or unsubstituted phenylene group; asubstituted or unsubstituted biphenylene group; a substituted orunsubstituted naphthylene group; substituted or unsubstituted alkenylenegroup; substituted or unsubstituted fluorenylene group; substituted orunsubstituted carbazolylene group; or substituted or unsubstitutedheteroarylene group having one or more of N, O and S atoms, Y1 is—N(Z1)(Z2), substituted or unsubstituted carbazole group, or substitutedor unsubstituted benzocarbazole group, Z1 and Z2 are the same as ordifferent from each other, and are each independently substituted orunsubstituted alkyl group; substituted or unsubstituted cycloalkylgroup, substituted or unsubstituted aryl group; substituted orunsubstituted alkenyl group; substituted or unsubstituted fluorenylgroup; substituted or unsubstituted carbazolyl group; or substituted orunsubstituted hetero ring group having one or more of N, O and S atoms,Y2 is hydrogen; deuterium; halogen group; nitrile group; nitro group;hydroxy group; substituted or unsubstituted alkyl group; substituted orunsubstituted cycloalkyl group; substituted or unsubstituted alkoxygroup; substituted or unsubstituted aryloxy group; substituted orunsubstituted alkylthioxy group; substituted or unsubstituted arylthioxygroup; substituted or unsubstituted alkylsulfoxy group; substituted orunsubstituted arylsulfoxy group; substituted or unsubstituted alkenylgroup; substituted or unsubstituted silyl group; substituted orunsubstituted boron group; substituted or unsubstituted alkylaminegroup; substituted or unsubstituted aralkylamine group; substituted orunsubstituted arylamine group; substituted or unsubstituted phenylgroup; a substituted or unsubstituted biphenyl group; a substituted orunsubstituted naphthyl group; substituted or unsubstituted fluorenylgroup; substituted or unsubstituted carbazolyl group; or substituted orunsubstituted hetero ring group having one or more of N, O and S atoms;and in the case of when two or more A, B, L1, L2, Y1 or Y2 are provided,they may be the same as or different from each other.
 2. The compoundaccording to claim 1, wherein Formula 1 comprises the following Formula2:

wherein at least one of R⁵ to R⁸, R′ and R″ is -(L1)p-(Y1)q, the remainsare each independently -(L2)r-(Y2)s, and X, L1, L2, Y1, Y2, p, q, r ands are the same as those defined by Formula
 1. 3. The compound accordingto claim 1, wherein Formula 1 comprises the following Formula 4:

wherein at least one of R⁵ to R⁸, R′ and R″ is -(L1)p-(Y1)q, the remainsare each independently -(L2)r-(Y2)s, and X, L1, L2, Y1, Y2, p, q, r ands are the same as those defined by Formula
 1. 4. The compound accordingto claim 1, wherein X of Formula 1 is selected from the substituentgroups described in the following [Table A-1]: TABLE A-1


5. The compound according to claim 1, wherein Y1 of Formula 1 isselected from the substituent groups described in the following [TableY-1]: TABLE Y-1 —Y1


6. An organic electronic device comprising: a first electrode; a secondelectrode; and one or more organic material layers that are disposedbetween the first electrode and the second electrode, wherein one ormore layers of the organic material layers comprises the compoundaccording to claim
 1. 7. The organic electronic device according toclaim 6, wherein the organic material layer comprises at least one ofthe hole injection layer and the hole transport layer, and at least onelayer of the hole injection layer and the hole transport layer comprisesthe compound that is represented by Formula
 1. 8. The organic electronicdevice according to claim 6, wherein the organic material layercomprises a light emitting layer, and the light emitting layer comprisesthe compound that is represented by Formula
 1. 9. The organic electronicdevice according to claim 6, wherein the organic material layercomprises the electron transport layer, and the electron transport layercomprises the compound that is represented by Formula
 1. 10. The organicelectronic device according to claim 6, wherein the organic electrondevice is selected from the group consisting of an organic lightemitting device, an organic phosphorescence device, an organic solarcell, an organic photoconductor (OPC) and an organic transistor.
 11. Thecompound according to claim 1, wherein Formula 1 comprises the followingFormula 3:

wherein at least one of R⁵ to R⁸, R′ and R″ is -(L1)p-(Y1)q, the remainsare each independently -(L2)r-(Y2)s, and L1, L2, Y1, Y2, p, q, r and sare the same as those defined by Formula 1, X is -(A)_(m)-(B)_(n),wherein m is an integer in the range of 1 to 10 and n is independentlyan integer in the range of 1 to 10, A is substituted or unsubstitutedphenylene group; a substituted or unsubstituted biphenylene group; asubstituted or unsubstituted naphthylene group; substituted orunsubstituted alkenylene group; substituted or unsubstitutedfluorenylene group having 13 to 30 carbon atoms; or substituted orunsubstituted heteroarylene group that comprises one or more of N, O andS atoms, B is deuterium; halogen group; nitrile group; nitro group;hydroxy group; substituted or unsubstituted alkyl group; substituted orunsubstituted cycloalkyl group; substituted or unsubstituted alkoxygroup; substituted or unsubstituted aryloxy group; substituted orunsubstituted alkylthioxy group; substituted or unsubstituted arylthioxygroup; substituted or unsubstituted alkylsulfoxy group; substituted orunsubstituted arylsulfoxy group; substituted or unsubstituted alkenylgroup; substituted or unsubstituted silyl group; substituted orunsubstituted boron group; substituted or unsubstituted phenyl group; asubstituted or unsubstituted biphenyl group; a substituted orunsubstituted naphthyl group; substituted or unsubstituted fluorenylgroup having 13 to 30 carbon atoms; or substituted or unsubstitutedhetero ring group having one or more of N, O and S atoms, in the case ofwhen A is substituted or unsubstituted phenylene group; a substituted orunsubstituted biphenylene group; a substituted or unsubstitutednaphthylene group; or substituted or unsubstituted fluorenylene grouphaving 13 to 30 carbon atoms, the number of carbon atoms of arylenegroup or fluorenylene group included in -(A)_(m) is 30 or less and B isdeuterium; halogen group; nitrile group; nitro group; hydroxy group;substituted or unsubstituted alkyl group; substituted or unsubstitutedcycloalkyl group; substituted or unsubstituted alkoxy group; substitutedor unsubstituted aryloxy group; substituted or unsubstituted alkylthioxygroup; substituted or unsubstituted arylthioxy group; substituted orunsubstituted alkylsulfoxy group; substituted or unsubstitutedarylsulfoxy group; substituted or unsubstituted alkenyl group;substituted or unsubstituted silyl group; substituted or unsubstitutedboron group; or substituted or unsubstituted hetero ring group havingone or more of N, O and S atoms, in the case of when B is substituted orunsubstituted phenyl group; a substituted or unsubstituted biphenylgroup; a substituted or unsubstituted naphthyl group; or substituted orunsubstituted fluorenyl group having 13 to 30 carbon atoms, the numberof carbon atoms of arylene group or fluorenylene group included in-(B)_(n) is 30 or less, A is substituted or unsubstituted alkenylenegroup; or substituted or unsubstituted heteroarylene group thatcomprises one or more of N, O and S atoms.
 12. The compound according toclaim 1, wherein Formula 1 comprises the following Formula 3:

wherein at least one of R⁵ to R⁸, R′ and R″ is -(L1)p-(Y1)q, the remainsare each independently -(L2)r-(Y2)s, and L1, L2, Y1, Y2, p, q, r and sare the same as those defined by Formula 1, X is -(A)_(m)-(B)_(n),wherein m is an integer in the range of 1 to 10, and n is independentlyan integer in the range of 1 to 10, A is substituted or unsubstitutedphenylene group; a substituted or unsubstituted biphenylene group; asubstituted or unsubstituted naphthylene group; substituted orunsubstituted alkenylene group; substituted or unsubstitutedfluorenylene group having 13 to 30 carbon atoms; or substituted orunsubstituted heteroarylene group that comprises one or more of N, O andS atoms, B is deuterium; halogen group; nitrile group; nitro group;hydroxy group; substituted or unsubstituted alkyl group; substituted orunsubstituted cycloalkyl group; substituted or unsubstituted alkoxygroup; substituted or unsubstituted aryloxy group; substituted orunsubstituted alkylthioxy group; substituted or unsubstituted arylthioxygroup; substituted or unsubstituted alkylsulfoxy group; substituted orunsubstituted arylsulfoxy group; substituted or unsubstituted alkenylgroup; substituted or unsubstituted silyl group; substituted orunsubstituted boron group; substituted or unsubstituted phenyl group; asubstituted or unsubstituted group; a substituted or unsubstitutednaphthyl group; substituted or unsubstituted fluorenyl group having 13to 30 carbon atoms; or substituted or unsubstituted hetero ring grouphaving one or more of N, O and S atoms, in the case of when A issubstituted or unsubstituted phenylene group; a substituted orunsubstituted biphenylene group; a substituted or unsubstitutednaphthylene group; or substituted or unsubstituted fluorenylene grouphaving 13 to 30 carbon atoms, m is 1 and B is deuterium; halogen group;nitrile group; nitro group; hydroxy group; substituted or unsubstitutedalkyl group; substituted or unsubstituted cycloalkyl group; substitutedor unsubstituted alkoxy group; substituted or unsubstituted aryloxygroup; substituted or unsubstituted alkylthioxy group; substituted orunsubstituted arylthioxy group; substituted or unsubstitutedalkylsulfoxy group; substituted or unsubstituted arylsulfoxy group;substituted or unsubstituted alkenyl group; substituted or unsubstitutedsilyl group; substituted or unsubstituted boron group; or substituted orunsubstituted hetero ring group having one or more of N, O and S atoms,in the case of when B is substituted or unsubstituted phenyl group; asubstituted or unsubstituted biphenyl group; a substituted orunsubstituted naphthyl group; or substituted or unsubstituted fluorenylgroup having 13 to 30 carbon atoms, n is 1 and A is substituted orunsubstituted alkenylene group; or substituted or unsubstitutedheteroarylene group that comprises one or more of N, O and S atoms. 13.The compound according to claim 1, wherein Formula 1 comprises thefollowing Formula 3:

wherein at least one of R⁵ to R⁸, R′ and R″ is -(L1)p-(Y1)q, the remainsare each independently -(L2)r-(Y2)s, and L1, L2, Y1, Y2, p, q, r and sare the same as those defined by Formula 1, X is -(A)_(m)-(B)_(n),wherein m is 1 and n is 1, A is phenylene group; biphenylene group;naphthalenyl group; fluorenylene group; substituted or unsubstitutedalkenylene group; or substituted or unsubstituted heteroarylene groupthat comprises one or more of N, O and S atoms, B is deuterium; halogengroup; nitrile group; nitro group; hydroxy group; substituted orunsubstituted alkyl group; substituted or unsubstituted cycloalkylgroup; substituted or unsubstituted alkoxy group; substituted orunsubstituted aryloxy group; substituted or unsubstituted alkylthioxygroup; substituted or unsubstituted arylthioxy group; substituted orunsubstituted alkylsulfoxy group; substituted or unsubstitutedarylsulfoxy group; substituted or unsubstituted alkenyl group;substituted or unsubstituted silyl group; substituted or unsubstitutedboron group; phenyl group; 1,2,3,4,5-pentadeuteriophenyl group;3-deuteriophenyl group; 3-fluorophenyl group; 2-cyanophenyl group;3-methylphenyl group; biphenyl group; stilbene group; naphthyl group;9,9-spiro bifluorenyl group; 9,9-diphenylfluorenyl group;9,9-dimethylfluorenyl group; fluorenyl group;spiro[cyclopentane-1,9-fluorene];2′3′-dihydrospiro[fluorene-9,1′-inden]; or substituted or unsubstitutedhetero ring group having one or more of N, O and S atoms.
 14. An organicelectronic device comprising: a first electrode; a second electrode; andone or more organic material layers that are disposed between the firstelectrode and the second electrode, wherein one or more layers of theorganic material layers comprises the compound according to claim
 2. 15.An organic electronic device comprising: a first electrode; a secondelectrode; and one or more organic material layers that are disposedbetween the first electrode and the second electrode, wherein one ormore layers of the organic material layers comprises the compoundaccording to claim
 3. 16. An organic electronic device comprising: afirst electrode; a second electrode; and one or more organic materiallayers that are disposed between the first electrode and the secondelectrode, wherein one or more layers of the organic material layerscomprises the compound according to claim
 4. 17. An organic electronicdevice comprising: a first electrode; a second electrode; and one ormore organic material layers that are disposed between the firstelectrode and the second electrode, wherein one or more layers of theorganic material layers comprises the compound according to claim
 5. 18.An organic electronic device comprising: a first electrode; a secondelectrode; and one or more organic material layers that are disposedbetween the first electrode and the second electrode, wherein one ormore layers of the organic material layers comprises the compoundaccording to claim 11.